November 23, 2024, 02:56:59 PM
Forum Rules: Read This Before Posting


Topic: Synthesis of 3-Carbethoxycoumarin  (Read 5492 times)

0 Members and 1 Guest are viewing this topic.

Offline mjb5676

  • Regular Member
  • ***
  • Posts: 9
  • Mole Snacks: +0/-0
Synthesis of 3-Carbethoxycoumarin
« on: November 10, 2012, 02:07:44 PM »
Can some one explain to me in detail the electron-pushing mechanism for the synthesis of 3-carbethoxycoumarin? The starting materials are salicylaldehyde, diethyl malonate, piperdine, and glacial acetic acid. they are all mixed in ethanol. I have the mechanism written down already, but I am not sure how to explain it.

Offline Dan

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 4716
  • Mole Snacks: +469/-72
  • Gender: Male
  • Organic Chemist
    • My research
Re: Synthesis of 3-Carbethoxycoumarin
« Reply #1 on: November 10, 2012, 02:21:09 PM »
To get you started: Enol

Have a go and show your attempt (this is a forum rule).
My research: Google Scholar and Researchgate

Offline mjb5676

  • Regular Member
  • ***
  • Posts: 9
  • Mole Snacks: +0/-0
Re: Synthesis of 3-Carbethoxycoumarin
« Reply #2 on: November 10, 2012, 05:19:19 PM »
I was thinking this was an aldol condensation reaction that formas an aldol. Then Dehydration then results in double bond formation and an α, β unsaturated compound. I lost internet connection a while ago before I wanted to pt a guess. Darn school.

Offline Dan

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 4716
  • Mole Snacks: +469/-72
  • Gender: Male
  • Organic Chemist
    • My research
Re: Synthesis of 3-Carbethoxycoumarin
« Reply #3 on: November 10, 2012, 06:06:50 PM »
Sounds good so far. This is known as a Knoevenagel Condensation.

So now you have ester and phenol functional groups and you want to form a lactone.

Hint: A lactone is a type of ester
My research: Google Scholar and Researchgate

Sponsored Links