April 28, 2024, 08:56:27 AM
Forum Rules: Read This Before Posting


Topic: Aspirin  (Read 4249 times)

0 Members and 1 Guest are viewing this topic.

Offline Super Newb

  • Regular Member
  • ***
  • Posts: 46
  • Mole Snacks: +1/-0
Aspirin
« on: August 26, 2012, 11:10:07 AM »
I am wondering if the sequence of oxidation or acylation will affect the overall synthesis. Any help will be appreciated :D

Offline discodermolide

  • Chemist
  • Sr. Member
  • *
  • Posts: 5038
  • Mole Snacks: +405/-70
  • Gender: Male
    • My research history
Re: Aspirin
« Reply #1 on: August 26, 2012, 11:12:17 AM »
I am wondering if the sequence of oxidation or acylation will affect the overall synthesis. Any help will be appreciated :D

I don't think your structures are correct!
You cannot acylate a methyl group with acetic anhydride/acetic acid.
The structure you drew is not aspirin which is acetyl salicylic acid
Development Chemists do it on Scale, Research Chemists just do it!
My Research History

Offline rrr_asd

  • Regular Member
  • ***
  • Posts: 15
  • Mole Snacks: +4/-2
Re: Aspirin
« Reply #2 on: August 26, 2012, 06:10:20 PM »
I think, it's must be correct.

Offline OC pro

  • Chemist
  • Full Member
  • *
  • Posts: 396
  • Mole Snacks: +36/-15
  • Gender: Male
Re: Aspirin
« Reply #3 on: August 27, 2012, 02:34:39 AM »
The first step will not work.

Offline IsotopeBill

  • Regular Member
  • ***
  • Posts: 35
  • Mole Snacks: +2/-1
Re: Aspirin
« Reply #4 on: August 27, 2012, 05:44:05 PM »
Do you have to start with phenol?  If so, look into ortho lithiation followed by treatment with an electrophile.

Offline Super Newb

  • Regular Member
  • ***
  • Posts: 46
  • Mole Snacks: +1/-0
Re: Aspirin
« Reply #5 on: August 28, 2012, 06:24:43 AM »
The first step will not work.

It is similar to the logic that aniline cannot be acylated and alkyalated by AlCl3 ? Much Thanks :D

Offline discodermolide

  • Chemist
  • Sr. Member
  • *
  • Posts: 5038
  • Mole Snacks: +405/-70
  • Gender: Male
    • My research history
Re: Aspirin
« Reply #6 on: August 28, 2012, 08:19:22 AM »
The first step will not work.

It is similar to the logic that aniline cannot be acylated and alkyalated by AlCl3 ? Much Thanks :D

The phenol will react!
Development Chemists do it on Scale, Research Chemists just do it!
My Research History

Offline Super Newb

  • Regular Member
  • ***
  • Posts: 46
  • Mole Snacks: +1/-0
Re: Aspirin
« Reply #7 on: August 28, 2012, 08:44:58 AM »
I am wondering if the sequence of oxidation or acylation will affect the overall synthesis. Any help will be appreciated :D

I don't think your structures are correct!
You cannot acylate a methyl group with acetic anhydride/acetic acid.
The structure you drew is not aspirin which is acetyl salicylic acid

I don't get what you mean by the the structure is wrong (isn't acetylsalicylic acid the same as aspirin)?


Offline curiouscat

  • Chemist
  • Sr. Member
  • *
  • Posts: 3006
  • Mole Snacks: +121/-35
Re: Aspirin
« Reply #8 on: August 28, 2012, 08:56:32 AM »
Quote
I don't get what you mean by the the structure is wrong (isn't acetylsalicylic acid the same as aspirin)?

The acetyl group you drew originally looks wrong.

Offline discodermolide

  • Chemist
  • Sr. Member
  • *
  • Posts: 5038
  • Mole Snacks: +405/-70
  • Gender: Male
    • My research history
Re: Aspirin
« Reply #9 on: August 28, 2012, 09:00:56 AM »
I am wondering if the sequence of oxidation or acylation will affect the overall synthesis. Any help will be appreciated :D

I don't think your structures are correct!
You cannot acylate a methyl group with acetic anhydride/acetic acid.
The structure you drew is not aspirin which is acetyl salicylic acid

I don't get what you mean by the the structure is wrong (isn't acetylsalicylic acid the same as aspirin)?



Check your structures they are incorrect.
You drew 2-(acetoxymethyl)benzoic acid not acetylsalicylic acid!
Development Chemists do it on Scale, Research Chemists just do it!
My Research History

Sponsored Links