synthetikal.com Forum Index


new p2p ?
Page 1 of 1
Post new topic   Reply to topic    synthetikal.com Forum Index -> Phenethylamines
Author Message
brain
Linguist Extraordinaire
Joined: 08 Mar 2005
Posts: 143
2405.16 Points

Mon Jun 06, 2005 1:51 am
Reply with quote

aldol condensation, benzaldehyde+methylethylketone katalized with HCl [oxidation bayer-viliger] , there is formed in situ par-acid from GAA and NaBO3n(H2O), hydrolisys with NaOH to P2P ....

sorry if i repeated post, but i didnt find it on this forum-can anyone help me? some more informations? mabey practical adwices? ewerything will hepl me !
Back to top
java
Consumer
Joined: 07 Feb 2005
Posts: 736
Location: The Mexican Republic
21796.14 Points

Mon Jun 06, 2005 4:04 am
Reply with quote

I found this at WD , it may be of some help or not............java
------------------------------------

mol of your favourite benzaldehyde
1.1 mol methyl or ethyl 2-chloropropionate
1.5 mol sodium methoxide, preferebly as the commercially avalible and dirt cheap 30% soln in MeOH.
Toluene, about 200-250 ml/mol benzaldehyde. Make sure the toluene is dry.

Add the toluene, benzaldehyde and haloester to a rb flask equipped with a mag stirbar, thermometer and a addition funnel. With cooling, add the sodium methoxide solution dropwise at a rate which keeps the reaction temperature between 10 to 15?C. When the addition is over allow the mixture to stir at room temp for one hour.
The toluene solution of the glycidic ester is now poured into 1 mol NaOH, as a 5% aqueous solution, and the mixture heated to 70-75?C for 60 minutes to hydrolyze the glycidic ester. The toluene layer is then separated from the aqueous layer. The sodium salt of the glycidic acid can now be isolated by concentration of the aqueous solution to about one third of the original volume and cooling to 10?C, filtration and washing with cold MeOH affords the salt in a quite pure form.

The phenylacetone is generated by heating the previous alkaline solution of the sodium salt of the glycidic acid to 90?C, and acidifying to pH 5.5 with either acetic acid or hydrochloric acid. A vigourous evolution of carbon dioxide starts immediately upon addition of acid. The slightly acidic solution is kept at 90?C for approximately one hour, or about 10 minutes after the carbon dioxide evolution has ceased. The solution is then cooled to room temperature, the pH raised to 8, and the ketone extracted with ether, DCM.
Back to top
Elementary

Joined: 18 Apr 2005
Posts: 100
Location: UK
3449.86 Points

Mon Jun 06, 2005 3:57 pm
Reply with quote

I'm sure this is being (been) discused elsewhere in this forum, try the search engine
Back to top
Display posts from previous:   
Post new topic   Reply to topic    synthetikal.com Forum Index -> Phenethylamines All times are GMT + 5.5 Hours
Page 1 of 1

 



Powered by phpBB 2.0.11 © 2001, 2002 phpBB Group

Igloo Theme Version 1.0 :: Created By: Andrew Charron