Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Mechanism
Butterfly
Harmless
*




Posts: 3
Registered: 14-1-2010
Member Is Offline

Mood: No Mood

sad.gif posted on 14-1-2010 at 14:22
Mechanism


I need some help with the mechanisms from structure 4 ---> 8 and from 9 ---> 3b. I am totally lost :(








Attachment: 1.docx (28kB)
This file has been downloaded 489 times
View user's profile View All Posts By User
Arrhenius
Hazard to Others
***




Posts: 282
Registered: 17-8-2008
Location: US & A
Member Is Offline

Mood: Stochastic

[*] posted on 14-1-2010 at 15:32


4 to 8 is nucleophilic attack of the amine lone pair on the acid chloride with addition/elimination to liberate a chloride ion which can deprotonate the ammonium ion to free HCL (hence the base present).

9 to 3b is oxidation of the enamine to the epoxide by oxone, coordination of the epoxide by sodium or potassium, and opening of the epoxide by attack of methanol followed by a proton transfer. Methanol attacks the more electropositive carbon adjacent to the nitrogen. The epoxide is initally formed anti to the ester due to unfavorable 1,3-pseudodiaxial interaction if you draw the enamine in the half chair (realistically the diastereoselectivity is probably poor). Nucleophilic opening of an epoxide must occur with anti-periplanar attack, so the methoxy group is initially "up", but presumably epimerizes here.

When you don't know a mechanism, the first thing to do is to try and identify a nucleophile and electrophile based on what you know about valence and electronegativity. Then 1.) make a bond 2.) break a bond 3.) draw the result. That being said, not all reactions involve nucleophiles/electrophiles.

[Edited on 14-1-2010 by Arrhenius]
View user's profile View All Posts By User
Butterfly
Harmless
*




Posts: 3
Registered: 14-1-2010
Member Is Offline

Mood: No Mood

[*] posted on 15-1-2010 at 02:50


Thank you so much for your complete answer :) But how does the oxone form the epoxide. I know that the active component of oxone is potassium peroxomomosulfate, KHSO5, but I can't draw the mechanism. Can you help me with that ?
View user's profile View All Posts By User
Arrhenius
Hazard to Others
***




Posts: 282
Registered: 17-8-2008
Location: US & A
Member Is Offline

Mood: Stochastic

[*] posted on 15-1-2010 at 06:18


http://en.wikipedia.org/wiki/Potassium_peroxymonosulfate

Just like with organic peroxyacids (e.g. mCPBA), oxone is an <b>electrophilic</b> reagent. So use the double bond as the nucleophile to attack the peroxide.

A mechanism as shown for mCPBA on wikipedia is probably sufficient. My only concern is that the proton transfer may not be intramolecular - this is trivial. Anyway, it's better to draw concerted addition of an oxygen atom to the alkene rather than a carbocation (don't draw these unless you have to).
http://en.wikipedia.org/wiki/MCPBA

[Edited on 15-1-2010 by Arrhenius]
View user's profile View All Posts By User
Butterfly
Harmless
*




Posts: 3
Registered: 14-1-2010
Member Is Offline

Mood: No Mood

[*] posted on 15-1-2010 at 06:59


Thank you so much. You are an angel :)
View user's profile View All Posts By User

  Go To Top