07-15-04 05:46
No 519570
Hello.
Is going from 4-Hydoxy-Tryptamine into 4-Hydroxy-DiMethylTryptamine possible via any of the routes used to go from tryptamine into dmt? as in this - ../rhodium /tryptam
Or is this completly impossible because the link between the HO molecule and the Carbon is too weak and will break when subjected to this kind of synthesis route?
(Hive Adickt)
07-15-04 06:14
No 519574
4-Hydoxy-Tryptamine into 4-Hydroxy-Tryptamine
huu ???
But yess, iff you have some 4-OH-tryptamine (lucky bastard) you can use the method in the link.
(Hive Bee)
07-15-04 07:05
No 519581
Post 127141 (ejlmp: "Psilocin in 5 steps", Tryptamine Chemistry)
By which method you want to synthesize the 4-hydroxy-indole?
The tendency is to push it as far as you can
(Stranger)
07-15-04 08:40
No 519591
I guess that the one who will choose to follow this reaction would like to purchase the 4-hydroxyindloe from a supplier.
(Hive Bee)
07-15-04 09:41
No 519599
Sorry, 4-hydroxy-tryptamine was meant of course....
Purchasing 4-hydroxy-indole/tryptamine is no good idea (in Lego's opinion) for two reasons:
1) the price
2) it is quite suspicious
Try unsubstituted tryptamine first....
The tendency is to push it as far as you can
(Stranger)
07-15-04 09:55
No 519602
I wonder what would be the effects of 6-ho-DMT if this compound was ever synthesized...
(Chief Bee)
07-15-04 12:33
No 519633
"It is pretty generally accepted that 6-HO-DMT is inactive. I am not too surprised. There are so few things with open and exposed hydroxyl groups that succeed in making it through the lipid barriers to the brain."
Alexander Shulgin in TiHKAL (http://www.erowid.org/library/books_onl
The Hive - Clandestine Chemists Without Borders
(Moderator)
07-15-04 12:57
No 519638
Beside that 4-OH-tryptamine is quite sensitive, especially even under slightly basic conditions. You would want to protect the hydroxy first with an apropriate group.