Author Topic: proscaline  (Read 1992 times)

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mysterious

  • Guest
proscaline
« on: February 26, 2003, 04:53:00 AM »
hi all friends!!

anyone every tried proscaline (p)?? i read of it in shulgins book!! do you know if this substance can be made of any uncontrolled substances??

anyone who tried it: how would  you describe the effects??

nice greetings!!
mysterious

Barium

  • Guest
Route
« Reply #1 on: February 26, 2003, 05:46:00 AM »
Syringaldehyde is alkylated with propyl iodide to 3,5-dimethoxy-4-propoxybenzaldehyde, the benzaldehyde is reacted with a chloroacetic acid ester in a Darzens condensation to give (3,5-dimethoxy-4-propoxyphenyl)acetaldehyde. This acetaldehyde can be reductively aminated with ammonia and Raney nickel, or the aldoxime formed with hydroxylamine which is then reduced to the amine proscaline (3,5-dimethoxy-4-propoxyphenethylamine). All reagents here are pretty unwatched.


Rhodium

  • Guest
syringaldehyde from vanillin
« Reply #2 on: February 26, 2003, 04:05:00 PM »
And syringaldehyde is easily made from vanillin:

https://www.thevespiary.org/rhodium/Rhodium/chemistry/mmda.mescaline.html


Antoncho

  • Guest
Questions, questions.
« Reply #3 on: February 26, 2003, 10:14:00 PM »
the benzaldehyde is reacted with a chloroacetic acid ester in a Darzens condensation to give (3,5-dimethoxy-4-propoxyphenyl)acetaldehyde. This acetaldehyde can be reductively aminated with ammonia and Raney nickel

Mmmmm, can you elaborate on that? Ever done this? I mean, you once wrote you were going to, but thus far all i read from you was on P2Ps via chloropropionates. Maybee, i should UTFSE better?

I always had a notion of this method as of somehow untrustworthy since those acetaldehydes would bee very hard to keep from polymerisation.... no?


Antoncho

Rhodium

  • Guest
Reductive amination of phenylacetaldehydes
« Reply #4 on: February 26, 2003, 10:33:00 PM »

hypo

  • Guest
easy is relative
« Reply #5 on: February 27, 2003, 12:53:00 AM »
> And syringaldehyde is easily made from vanillin:

iirc some bees (antoncho?) have had problems with the
methoxylation step.

uemura had big problems separating OH-vanillin from vanillin.
(ok, that's not syringaldehyde, but related)

i don't consider those syntheses "easy".
(for otc-bees. now if you have high grade chemicals it's probably a breeze...)