L42L (Stranger)
05-18-04 03:08
No 507814
      novel newbee tryp decarb question session     

This was passed on to me

“Tell me what cha think,

In a microwave reflux situation, tryptophan (about 7g) is refluxed in glycerin (about 125 mL) with a small amount of enone (pugelone) until no more gas comes out top of condenser, takes a few minuets for this to happen. As solution is heated, tryptophan appears to dissolve and solution begins to take on a dark reddish brown color. As this occurs there is the definite smell of something “DMT-ish” Solution is cooled, it is a deep dark rust color.

Solution is around ph 7.4 or 7.8 (author can’t remember what was told) Solution is then basified with saturated NaOH solution, pH is 11.5. What looks like some whitish-yellow substance has come out of solution. Solution is diluted with a small amount of H2o and thrown in to sep funnel. An amount of chloroform is added and sinks to bottom. Sep gets well shaken. The result is a clump of red-brown stuff floating about with the rest of solution now a lighter color of rusty orange-yellow. At the bottom of sep is a small amount of chloroform, noticeably less than what was originally put in, it is a rusty orangey color.

A small amount of the sticky brown stuff is taken out and subject to muritic acid and then boiling chloroform, both seem to have no effect on the substance (it does slightly color the chloroform yellow).

Should be noted that the individual has smelled free-base DMT but no other indole before (except tryptophan) The size of the brown lump is about the same size as the original amount of tryptophan.

Is glycerin a suitable for this?

Is this appropriate reasoning?>If one has an amine in an alcohol, then basifiy and extract with nonpolar solvent to get amine.

Was it over basified (too high pH) or too strong of base (saturated NaOH)?

Is that brown clump a nasty tar?

It seems strange that there is less chloroform than what was originally added.

What kind of crazy side reactions could be going on?

Does tryptamine smell like DMT, is that smell particular to indoles in general?

Can this be saved?

Sorry if this seems rushed, it is.”

So…….from this small amount of info any bee have any comments?
Thank you so much, any thoughts and speculations are welcome.
 
 
 
 
    Novice
(Newbee)
05-18-04 12:12
No 507873
      ...     

"Is glycerin a suitable for this?"

As glycerine decomposes upon boiling at atmospheric pressure I'd say no, not really.

"Is this appropriate reasoning?>If one has an amine in an alcohol, then basifiy and extract with nonpolar solvent to get amine."

Generally no, since many alcohols are soluble in the NP (glycerol is not soluble in chloroform however). Getting rid of the alcohol and keeping the water, then extract with NP is the usual way to go.

"It seems strange that there is less chloroform than what was originally added."

Some of the NP will dissolve in the water phase, it's not a problem if you do several extractions though.

"Can this be saved?"

There are lots of functional routes on The Hive, UTFSE and you'll see...
 
 
 
 
    ning
(acetaminophanatic)
05-18-04 16:05
No 507893
      Mineral oil is a good solvent for this kind of     

Mineral oil is a good solvent for this kind of thing. It's inert, clean, and very high boiling AFAIK.

...it's an AOL chatroom for dyslexic spider monkies...
 
 
 
 
    Erny
(Earnest Bee)
05-18-04 17:40
No 507905
      Re: decarb question session     

Was it over basified (too high pH) or too strong of base (saturated NaOH)?

Possibly yes, chloroform, upon contact with concentrated alkali, forms dichlorocarbene.

What kind of crazy side reactions could be going on?


Alpha-aminoacids turn into cyclic diketopiperazines when heated to a too high temp. Chloroform with alkali and primary amines could form isonitriles.

Does tryptamine smell like DMT

Tryptamine, as well as DMT and DET smells like plastic. The smell differs a little from one substance to another.

is that smell particular to indoles in general?


No smile

From SWIM's experience, procedure with cyclohexen-2-one in cyclohexanol worked, but his maximum yield was 5,5 g of the tryptamineHCl from 15 g D,L-tryptophan, possibly due to overacidifying and heating TxHCl in an aqueous hydrocloric acid for some time during the workup. All the tryptophan did not dissolve during the decarboxylation, half of it remained unchanged after the sixth hour.

Swim wonders about possible mechanism of this reaction. Could imine, where the lone pair of amine nitrogen is delocalised on that double bond of ketene, be one of the important intermediates?
 
 
 
 
    armageddon
(Hive Bee)
06-27-04 15:54
No 515774
      OK here are my personal tryp decarb newbee...
(Rated as: UTFSE!)
    

OK here are my personal tryp decarb newbee questions:

Does anyone know if MEK can be used instead of cyclohexenone? If this is the case: which solvent should be used then? Tetralin? Or maybe toluene/xylene? What about high boiling alcohols like n-nonanol (bp 215°)?

THX A

"..ein Trank von unterschiedlicher Farbe, in ihm ist Heilung fьr die Menschen."
 
 
 
 
    Novice
(Hive Bee)
07-05-04 15:06
No 517551
      Won't do.     

MEK and xylene/toluen won't work. Xylene and toluene have too low boiling points, not to mention MEK. I've tried it, the yield was about 2% or so.

Use MDP2P in tetralin, it should work coolwink
 
 
 
 
    Vitus_Verdegast
(Hive Addict)
07-05-04 15:33
No 517555
      this reaction is much trickier than it seems..     

All these were tried by Yours Truly, and only resulted in tar, unreacted tryptophan, very low yields to no product at all, and the ever-present lingering smell of skatole:

DMSO/Trp copper chelate, DMSO/acetone, DMSO, turpentine/d-carvone, acetophenone and pyrolysis under vacuum.

It's amazing how much frustration this "simple decarboxylation" has cost me.

http://www.mindspring.com/~rathcoombe/horror/raven2.jpg
 
 
 
 
    L42L
(Newbee)
07-06-04 18:07
No 517764
      Oh my     

turpentine/d-carvone

didnt work? at all? that was to bee the last resort, ala "student"(see tryp decarb at rhodium)any details you feel like sharing are still appreciated

vary lame
 
 
 
 
    Vitus_Verdegast
(Hive Addict)
07-06-04 20:07
No 517770
      not for me     

But looking back I now have the impression that my stirring wasn't efficient enough. For Student's procedure you certainly need good overhead stirring.

http://www.mindspring.com/~rathcoombe/horror/raven2.jpg
 
 
 
 
    L42L
(Newbee)
07-06-04 23:09
No 517801
      strange     

would never think that that would be an issue, as long as there is nice reflux
 
 
 
 
    Vitus_Verdegast
(Hive Addict)
07-06-04 23:51
No 517806
      there is an issue     

As tryptophan will not dissolve in hot turpentine, you need to have a constant even distribution as you want as much surface area as possible exposed to the ketone-containing solvent, so that it can form the imine in a steady manner. Next to that, it will help a lot to drive the CO2 out of the reaction mixture.

If you omit stirring, you will encounter heavy bumping and the process will take forever and a day to complete.

http://www.mindspring.com/~rathcoombe/horror/raven2.jpg
 
 
 
 
    _mu_
(Hive Bee)
07-07-04 21:43
No 517992
      Are there any reports of people who have ...     

Are there any reports of people who have gotten this reaction to work? So far I've only read about failures.
 
 
 
 
    dennis_pro
(HyperLab Bee)
07-08-04 08:26
No 518120
      me     

I'm successfully decarboxylated DL-tryptophan (DMSO, menthone+acetone). Reaction completes at half a hour.
Pictures and procedure (w/pictures, on russian): Post 509654 (dennis_pro: "Иллюстрированное декарбоксилирование", Russian HyperLab).

With best regards,
Dennis Prochko aka Wolf
 
 
 
 
    _mu_
(Hive Bee)
07-08-04 09:03
No 518125
      Your reaction mixture seems to be reddish...     

Your reaction mixture seems to be reddish right from the start. What's the trick to get it working?
 
 
 
 
    Lilienthal
(Moderator)
07-08-04 10:15
No 518131
      How have you tested if it is indeed tryptamine     

How have you tested if it is indeed tryptamine and not a cyclization product?
 
 
 
 
    Vitus_Verdegast
(Hive Addict)
07-08-04 17:22
No 518171
      tryptamine carbonate     

Post 512109 (jemma_jamerson: "purifying tryptamine and co2", Tryptamine Chemistry):


Patent US2943093 gives a method for purifying tryptamine compounds by treatment with CO2 in a solvent to form the carbonate which precipitates from the solution. CO2 is in the air. I wonder if this could cause problems when handling tryptamines. Tryptamine carbonates tend to be insoluble in solvents like alcohol and methylene dichloride. Heating the tryptamine carbonate decomposes it into the tryptamine and CO2.




Maybe you should try this out on the product you've obtained..


http://www.mindspring.com/~rathcoombe/horror/raven2.jpg
 
 
 
 
    Vitus_Verdegast
(Hive Addict)
07-08-04 18:33
No 518179
      crude translation of dennis_pro's post     

My Russian isn't what it used to be anymore smile, but here is a translation of Dennis_pro's post:
(I'll include the pictures too)




dennis_pro
(HyperLab Bee)
05-26-04 05:23
Post 509654 (dennis_pro: "Иллюстрированное декарбоксилирование", Russian HyperLab)
Illustrated decarboxylation
(Rated as: excellent)

As the catalyst was used menthone, which was obtained by the oxidation of menthol using potassium dichromate in the presence of sulfuric acid, employing the general procedure as described in Organikum.


20 g DL- tryptophan was placed into the flask, equipped with a reflux condenser and stirrer (? don't see one on the pictures -VV) , and there was added 50 ml of dimethylsulfoxide (pharmaceutical grade "dimexid"), followed by a solution of 0.5 ml menthone in 5 ml of acetone, and, using good stirring (caution: evolution of carbon dioxide, strong frothing!) was heated to 150-180°C for an hour (actually the reaction already subsided after 30 min).
(That last part of the sentence, is that correctly translated? "нагревают при 150-180С в течение часа"))


30 minutes after the reaction started boiling, there was added through the condensor 5 additional ml of acetone (the vapors of acetone protect the reaction mixture from oxidation by atmospheric oxygen). When the reaction was finished, the solution became completely transparent and the evolution of carbon dioxide ceased.


The resulting pink coloured solution was allowed to cool and was diluted with 200 ml water, causing the mixture to become cloudy and the base of tryptamine is liberated in the form of a red oil.


70% acetic acid was added which led to the complete dissolution of oil. This was neutralized with sodium bicarbonate until no more CO2 was evolved. This caused part of resins to float together with the foam. The mixture was filtered through cotton, which removed floating resins. Nevertheless, the solution remained a red color. For a more complete removal of resins the mixture was washed with a small quantity of dichloromethane.


Aqueous NaOH was added, which caused the mixture to become cloudy, and after standing overnight tryptamine precipitated, which was filtered off and dried. Tryptamine obtained this way will still contain traces of NaOH. Attempts at washing the precipitate on the filter with water will lead to the significant losses of tryptamine as a result of its significant solubility in the water (34 g/l).


Since tryptamine possesses significant solubility in the water, it is better to extract the resulting alkaline suspension of tryptamine three times with benzene. Extracts are pooled and dried with anhydrous MgSO4, and to this is added just enough petroleum ether to turn the solution cloudy, and the solution is left overnight in the refrigerator. During the night tryptamine is crystallized in the form of completely colorless needles.

/zavtra I will report this fotku, forgot krassota:) / The general output not of schitan, since with the experiments separation of candy (tryptamine) from govna resin) product threw out itself on nemnogu into the toilet. Procedure will be improved on the following week, with the application of the almost inert gas:)

P.S. The use of the organic (?) solvents, acetic acid and bicarbonate is compulsory, an attempt at the acidification by sulfuric acid, and the extraction of resin by petroleum ether did not succeed, since resins and tryptamine in it were left mostly undissolved.
Attempts to directly basify the solution and to immediately extract tryptamine with benzene lead to the isolation of red noncrystallizing resin:




wink

http://www.mindspring.com/~rathcoombe/horror/raven2.jpg
 
 
 
 
    GC_MS
(Hive Addict)
07-08-04 19:42
No 518186
      Rrrrrussia     

Muito agradбvel! Vitus, vocк й o mais melhor! laugh

Aztecunnilingus Maximus
 
 
 
 
    L42L
(Newbee)
07-08-04 20:05
No 518193
      FOOK YA!!! (i hope)     

ok, dare i ask? yes, what are the yields?
 
 
 
 
    Vitus_Verdegast
(Hive Addict)
07-08-04 20:14
No 518196
      From Rrrraaashhia with love ;-)     

Dos Agradecimentos GC_MS! laugh

Now, my impression is that the small amount of menthone is not the relevant ketone, but much more so acetone, although considering its low boiling point this would be quite unlikely too.

Let's say there is 3 mmol of menthone available for every 100 mmol tryptophan, compared to the 68 mmol acetone in which the menthone was added. Maybe it would be a good idea to add 5 ml acetone every 5 minutes or so?

Also... --> из триптамина выход? smile
You didn't tell us what your final yield was..

http://www.mindspring.com/~rathcoombe/horror/raven2.jpg
 
 
 
 
    Vitus_Verdegast
(Hive Addict)
07-08-04 20:58
No 518202
      Another failure with Student's procedure     

This is the translation of the first post in that thread, by Erny, who tried Student's procedure and failed.



Erny
(Earnest Bee)
12-13-03 16:52
Post 476610 (Erny: "Декарбоксилирование триптофана a la Student", Russian HyperLab)

Decarboxylation of tryptophan a la student

The procedure, outlined in ../rhodium/hyperlab/syntheses/tryptophane_.decarbox.htm did not bring a desired result when performed under our conditions.

15 g of tryptophan, 150 ml of the turpentine, purchased in the economic store, and 30 drops of pharmaceutical peppermint essential oil were placed into a 250ml Erlenmeyer flask and the mixture was heated to reflux while stirring magnetically. After 18 hours of reflux, unreacted tryptophan was filtered off on the Buechner and washed with 70 ml of dichloromethane. The yellow turpentine motherliquor and dichloromethane washing were pooled and extracted with 5% aqueous HCl, this was basified with potassium hydroxide to pH ~12 and extracted with approximately 100 ml of benzene. Extracting this again with 5% aqueous HCl showed no amines were present at all.

The unreacted tryptophan had a white color and it weighed 14.2 g, that, taking into account losses on filtering, it appears that no decarboxylation reaction took place at all, and generally tryptophan remained unchanged in the reaction mixture.

If someone has positive ideas as how to tackle the decarboxylation of tryptophan, express them, if you please.




You HyperLab bees should share abit more information like this with us smile.
From now on you can expect me to come looking in there from time to time wink...


EDIT: Of course, there is not enough ketone present here too, since peppermint essential oil contains anywhere from 10-50% menthone..
http://www.millenniumchem.com/NR/rdonlyres/6C43C1E8-EFAD-42E4-8357-4A519E99B743/0/PEPPERMINTOIL540.pdf

http://www.mindspring.com/~rathcoombe/horror/raven2.jpg
 
 
 
 
    _mu_
(Hive Bee)
07-08-04 23:33
No 518236
      IIRC, the ketone acts as a catalyst.     

IIRC, the ketone acts as a catalyst. So you don't actually need equimolar amounts of ketone.
 
 
 
 
    Vitus_Verdegast
(Hive Addict)
07-08-04 23:47
No 518243
      as I understand it     

The tryptophan forms an unstable ketimine with the ketone, which readily decarboxylates giving the imine of tryptamine. After hydrolysis you have tryptamine and ketone again.

But some ketones like acetophenone will give stable imines with tryptamine, which will not readily hydrolize unless you heat them in an acidic or basic environment.

I don't know about menthone, but the imine from tryptamine and acetone should be much more readily hydrolyzed. If the imine from menthone and tryptamine would not be readily hydrolyzed, it wouldn't be much of a catalyst.


Next to this, there is the additional problem, that with some ketones, transamination may occur.

http://www.mindspring.com/~rathcoombe/horror/raven2.jpg
 
 
 
 
    Rhodium
(Chief Bee)
07-09-04 01:21
No 518262
      These recent posts explains a lot of stuff     

Post 509761 (Nicodem: "Mechanism of decarboxylation literature", Tryptamine Chemistry)
Post 509782 (Rhodium: "Catalytic transamination/decarboxylation cycle", Tryptamine Chemistry)

The Hive - Clandestine Chemists Without Borders
 
 
 
 
    L42L
(Newbee)
07-09-04 01:52
No 518267
      compulsory     

"
P.S. The use of the organic (?) solvents, acetic acid and bicarbonate is compulsory, an attempt at the acidification by sulfuric acid, and the extraction of resin by petroleum ether did not succeed, since resins and tryptamine in it were left mostly undissolved.
Attempts to directly basify the solution and to immediately extract tryptamine with benzene lead to the isolation of red noncrystallizing resin:
"

WTF, would never guessed, so on that note i have to ask;
can one assume that good old 5% acetic is fine for this?
 
 
 
 
    dennis_pro
(HyperLab Bee)
07-09-04 02:48
No 518283
      Thanks, bees     

Thanks all, here it is some my comments.

_mu_:

Your reaction mixture seems to be reddish right from the start. What's the trick to get it working?



The reaction brings some reddish color immidiately after heating to 150 C. Some tryptophan dissolves, evolution of CO2 starts and mix brings some reddish. No special tricks.

Lilienthal:


How have you tested if it is indeed tryptamine and not a cyclization product?


I haven't measure the melting point of the product (i haven't a thermometer :(), but all phys-chem properties shows that it is tryptamine. Moreover, it was alkylated with EtBr and the products was show the activity. I planned some experiments in future, where all will be measured right.

Vitus_Verdegast:
Nice translation, thanks.


don't see one on the pictures


Yes, the stirring was completed by hands when the foam rised up to condenser.


That last part of the sentence, is that correctly translated?


Yes, this is correct.


The general output not of schitan, since with the experiments separation of candy (tryptamine) from govna resin) product threw out itself on nemnogu into the toilet.


Politicaly correct translation is: "The total yield was not calculated, since during of the reaction workup (purifying the tryptamine from the resin byproducts), much of the reaction mixture was discarded"


The use of the organic (?) solvents


Correct.


You didn't tell us what your final yield was



The total yield i obtained was 2g (from 20g tryptophan). But much, very much of the reaction mixture was discarded when i was tried to remove resins by recrystallization, A/B reextraction, trying various solvents, etc. You can obtain good results with using of inert gas and provided instructions. (My workup was completed during 2 days, without protection reaction mixture from air: slightly reddish reaction mixture makes intensively red after these days. Oxidation?)

Future questions are welcome. Thanks again.

P.S. Sorry for my terrible english.


With best regards,
Dennis Prochko aka Wolf
 
 
 
 
    Erny
(Earnest Bee)
07-09-04 12:25
No 518368
      Decarboxylation with cyclohexen-2-one     

The first attempt of tryptophan decarboxylation was described at Post 478376 (Erny: "Декарбоксилирование триптофана - бета версия", Russian HyperLab) (1)

Here I'll describe the second:

In a 250 ml erlenmeyer flask there were added 15 g of D,L-tryptophan along with 150 ml of cyclohexanol and 2 ml commercial cyclohexen-2-one. A reflux condenser was attached and the RM was brought to reflux while stirring magnetically. Warm water was used in the reflux condenser as, when using cold water, cyclohexanol crystallized in it. After 2,5 h of reflux only about a half of the tryptophan had dissolved, and the RM was orange. It was cooled to approx 50°C and as the air went into the flask the RM turned brown. 50 ml of petroleum ether (2) and 200 ml of diluted hydrochloric acid were added, layers were separated and the slightly acidic water layer (3) was evaporated to give 9 g of brown sparkling crystalline mass. After grinding it with acetone, filtering on buechner and washing with acetone it became pink, was turned into freebase and recrystalized from benzene (4). 3,7 g of white sparkling sugar-like crystals were obtained. It's mp was correct and DMT was made from it a la Shulgin wia the ethylformiate/LAH route.

Notes:

1. In the first attempt 15 g of tryptophan, 1,5 ml of cyclohexen-2-one and 150 ml of cyclohexanol were used. Reaction time was 6,5 h and the final yield of tryptamine - 3,3 g.
2. Petroleum ether was added for the better separation of phases.
3. To evaporate the acidic solution was a great mistake: when almost all of the water was gone, pH was already <2 and it dropped the yield more than twice (as can be seen from the amount of hydrochloric acid used to neutralise the tryptamine during the extraction).
4. Dichloromethane may be used instead of benzene. The best solvent for the extraction of tryptamines is EtOAc.
5. The solvents/reagents were not dried and, as the water is present in the equilibrium amine + ketone <__> imine + H2O, drying may also improve the yield.
 
 
 
 
    Lilienthal
(Moderator)
07-09-04 13:36
No 518376
      It has been shown (UTFSE for different melting     

It has been shown (UTFSE for different melting points of tryptamine) that recrystallization from acetone produces the corresponding imine, not the free tryptamine.

Any imine of tryptamine is prone to cyclization under acidic conditions, resulting in tetrahydro-beta-carbolines which are still amines and behave like amines.

Maybe the conjugated doublebond from alpha-beta-unsaturated ketones inhibita this cyclization a bit.  Howower, I would suggest to remove any trace of ketone before acidifying the workup solution.
 
 
 
 
    dimitry
(Stranger)
07-21-04 14:14
No 520592
      Decarboxilation in o-xylol
(Rated as: good read)
    

Hi all.
SWIM successfully decarboxilated tryptofan in o-xylol.
There is description it synthesis:
3g pure tryptofane suspended in 10ml o-xylol and about 3ml acetophenone. Its mixture refluxed 25-35 hours(with interruptions),almost tryptophane was dissolved. Rm cooled to 50-60C and tryptamine was extracted  3*10ml 10%HCl at heating( In order to Shiff-base hydrolized heating need.).Acid solution was basified and tryptamine  was extracted with  CHCL3. Solvent was distilled on water bath and tryptamine (about1.2-1.3g) was yielded. that is tryptamine was successfully methylated and ethylated  to dmt,det.