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lutesium
(Stranger) 06-22-04 03:54 No 514705 |
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Mescaline Advice Needed | ||||||
This is my first post to my one and only love - THE HIVE..!! (Im UTFSE ing for 2 YEARS without a making single post so dont flame me. I really need your advice.) Swim wants your advice for the best route to mesc. starting from pyrogallol. For reduction Na metal or NaBH4 can be used. Shoud you Pyrogallol---+dimethyl sulfate-> Trimethoxy pyrogallol --halomethylation-> 2,3,4 Trimethoxy Benzyl Bromide ---NaCN---> 2,3,4 Trimethoxy Benzyl Cyanide ---H--> Mesc or is there another way which seems better (easier and higher yielding) to you? Especially the bromomethylation and with playing w/ NaCN seems problematic to swim but he did it before for many times and he can handle. Just give me some advice and I would be grateful if you link me to some good posts about this subject. Thanx |
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java (Hive Bee) 06-22-04 04:46 No 514717 |
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mescaline advice... | ||||||
Read about what some have to say about your route proposed....... Post 303631 (zed: "Not easy!", General Discourse) some suggestions..... Post 304555 (zed: "Maybe.", General Discourse) ../rhodium /mescaly ../rhodium /mescali here is another place to look... http://www.mescaline.com/synth/ http://www.maps.org/forum/1998/msg00321. this should get you going.........java Just hold on to the thread...that keeps us going http://www.chiapaslink.ukgateway.net/ |
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Rhodium (Chief Bee) 06-22-04 04:46 No 514718 |
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UTFSE! | ||||||
Post 514603 (Mephisto: "Scan: TMBA from Vanillin - Synthesis 308 (1983)", Chemistry Discourse) Post 514141 (psyloxy: "3,4,5 precursors revisited", Chemistry Discourse) Post 514596 (Rhodium: "Many routes to 3,4,5-Trimethoxybenzaldehyde", Methods Discourse) Post 345054 (slothrop: "3,4,5-TMB from p-Cresol", Methods Discourse) The Hive - Clandestine Chemists Without Borders |
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xxxxx (Hive Bee) 06-22-04 20:54 No 514807 |
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don't start from pyrogallol | ||||||
i have read that 2,3,4-trimethoxy phenethylamine is inactive, however 2,3-methylenedioxy 4-methoxy phenethylamine is active. this was plausibly explained as being because the rotation of the 2-methoxy group interfers with the ethylamine when it is binding to the receptors, when this is constrained as a 2,3-methylenedioxy ring activity is preserved. if you have 3,4,5 trimethoxy gallic acid maybe you could 1)condense the ethyl ester with ethyl acetate using sodium ethoxide to form (ch3o)3c6h2coch2cooc2h5 2)reduce the ketone to (ch3o)3c6h2ch2ch2cooc2h5 3)add ethanolic ammonia to form (ch3o)3c6h2ch2ch2conh2 4)add naocl to form (ch3o)c6h2ch2ch2nh2. i have posted this elsewhere and people said it might work. if it doesn't you probably won't be as badly off as if you used a process involving cyanide. |
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Rhodium (Chief Bee) 06-22-04 21:36 No 514813 |
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4-Methoxy-2,3-Methylenedioxy-PEA | ||||||
i have read that 2,3,4-trimethoxy phenethylamine is inactive, however 2,3-methylenedioxy 4-methoxy phenethylamine is active. What is your source for that statement? I can only find four literature citations on the latter compound, and as far as I know the substance has never been tried in man. 4-Methoxy-2,3-Methylenedioxy-PEA: Heterocycles 45(9), 1751-1758 (1997) Phytochemistry 28(7), 1967-1972 (1989) Chem.Nat.Compd.(Engl.Transl.); EN; 21; 6; 1985; 777-782; (Khim.Prir.Soedin.; RU; 6; 1985; 818-823) Chem.Nat.Compd.(Engl.Transl.); EN; 29; 3; 1993; 341-345; (Khim.Prir.Soedin.; RU; 3; 1993; 404-409) The Hive - Clandestine Chemists Without Borders |
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xxxxx (Hive Bee) 06-22-04 23:17 No 514826 |
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read it in a book | ||||||
i can't provide the reference for this statement. even if i could it would likely be difficult to locate the citation. anyway 2,3,4 trimethoxy phenethylamine is not mescaline. |
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lutesium (Stranger) 06-22-04 23:39 No 514833 |
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Oh all my fault I didnt mean 2,3,4 rather 3,4,5 | ||||||
Thanks for all replies you've been really helpful showing me alternatives to the undeliciate route to I proposed And I would like to read some articles about the drug-receptor-effect relationship especially over the phenethylamine or indole releated. I have questions bugging my mind like say what that 4- position means to someones brain creating different effects over the same molecule or say what does the length of a hydrocarbon chain means to the receptors? What are the strategy/methodology for rhe creation of phenethylamine derivatives and so on If you have these kind of articles to post/link here I would appreciate it SOOOO much |
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Rhodium (Chief Bee) 06-23-04 03:53 No 514871 |
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Structure-Affinity Relationships (SAR) | ||||||
I believe that you are looking for these threads: Post 500985 (Rhodium: "Shulgin: 90 pages of Psychedelic SAR", Serious Chemistry) Post 453382 (Rhodium: "Related SAR article, with DOF/DOI/DON synth", Serious Chemistry) The Hive - Clandestine Chemists Without Borders |
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hest (Hive Adickt) 06-23-04 12:51 No 514957 |
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2,3,4-PEA | ||||||
Are we talking abouth this one ?? Pihkal #91 IM (Isomescaline; 2,3,4-Trimethoxyphenethylamine) (http://www.erowid.org/library/books_onl |
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chilly_willy (Hive Bee) 06-23-04 21:24 No 515012 |
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start.. | ||||||
Try this... vanillin --> bromovanillin --> hydroxyvanillin --> TMBenzaldehyde -->TMBnS-->Mescaline via. Zinc/HCl ala. leminger (search Rhodium). The only real problems here would be the labor involved and acquiring either DMSulfate/MeIodide. Everything else required can be obtained locally or through the normal routes. If you look hard enough it might even be possible to locate the trimethoxybenzaldehyde commercially..and from there it would be two relatively easy steps. The shortest distance between two points is a straight line |
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lutesium (Stranger) 06-23-04 23:21 No 515038 |
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thank you all.!!! | ||||||
Thank you all for your replies. Without you I would try for at least a week to achieve this much info. (AND SAR IS GREAT!! ) But swim has a uncommon problem. has dms, a fumehood and a good place to work but he cannot obtain any nitromethane cuz its forbidden. He will run the experiment at most 10gr scale for once and he doesnt need much nitro he knows.. but there is none and none is none. Making it is also a hassle as much as I know from Kolbes synth starting from chloracetic acid. Making the latter percusor is hard and its too expensive to obtain for such small yields that wont even make you feel to distill it :( I searched for many weeks and read most threads about the R-No2 stuff but none of the routes seem appealing. Is there something that Im missing? If the r-no2 problem is solved swim also has ethylenediamine |
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hest (Hive Adickt) 06-24-04 12:31 No 515130 |
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? | ||||||
Are you asking us to mail you a sample ????? ../rhodium /nitroal Don't know where you live, but it is OTC in manye part of the world (hi octane fuel ect) |
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lutesium (Stranger) 06-24-04 18:21 No 515160 |
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no I didnt mean that | ||||||
I just wanted you to post a route that will start the you know: Read, get excited, go out, purchase, synth. , get excited again " cycle. No route is "so great" to cause swim to even try (even when in a manic state where anything seems possible but r-No2 dont :( |
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lutesium (Stranger) 06-24-04 18:41 No 515162 |
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DMS Route seems acceptable but they say ... | ||||||
DMS Route seems acceptable but they say shake?? stirring the dms+nano2 will be sufficent I think. Is this true? |
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cattleprodder (Hive Bee) 06-26-04 10:43 No 515525 |
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start with 3,4,5-trimethoxybenzaldehyde. | ||||||
Problem #1: You don't have 3,4,5-trimethoxybenzaldehyde right now. Like chilly_willy said, do some internet searching for OTI (over the internet) 3,4,5-trimethoxybenzaldehyde. This is the first step which will save you much trouble later on, as the battle to synth M will be 1/2 way won as soon as your package arrives. Make sure you find a shady source. Problem #2: You can't get nitromethane. In the latter case you have pretty much already answered this dilemma in your very first post of this thread. Namely, 3,4,5-trimethoxybenzaldehyde plus sodium borohydride followed by thionyl chloride followd by sodium cyanide followed by lithium aluminum hydride. It can be done this way, but if I were you I would research the ingredients of commercially available race car fuel before giving up on the MeNO2 route. Happy Mescaline Chasing |
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lutesium (Stranger) 06-27-04 20:47 No 515847 |
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thanx for reply | ||||||
Your advices offered me a wide range of possiblities much thanks. I found out that my local chem company offers nitroalkanes in 250ml quantities along with the 3,4,5 trimeo bzal so this synth will be easy. Can you lead me to some imformative posts about the condensation considering that swim has ethylenediamine if it offers an advantage. Thanx Love You |
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moo (Hive Bee) 06-27-04 21:51 No 515863 |
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Your local chem company might also have an... | ||||||
Your local chem company might also have an idea of what those chemicals can be used for. fear fear hate hate |
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GC_MS (Hive Addict) 06-27-04 22:28 No 515867 |
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M | ||||||
I found out that my local chem company offers nitroalkanes in 250ml quantities along with the 3,4,5 trimeo bzal so this synth will be easy. Can you lead me to some imformative posts about the condensation considering that swim has ethylenediamine if it offers an advantage. Mescalinic benzaldehyde ( ![]() ![]() And if you still plan to order it from your supplier, at least be wise enough NOT to order these compounds from the same supplier in the same order. You'd be asking from troubles. Aztecunnilingus Maximus |
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java (Hive Bee) 06-30-04 22:29 No 516599 |
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mescaline advice... | ||||||
As I was going through the files I read this and thought of your project.......java Post 414469 (Vitus_Verdegast: "alternative routes to mescaline", Novel Discourse) Just hold on to the thread...that keeps us going http://www.chiapaslink.ukgateway.net/ |
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