December 27, 2024, 04:43:57 AM
Forum Rules: Read This Before Posting


Topic: Sulfoxide elimination  (Read 7672 times)

0 Members and 2 Guests are viewing this topic.

Offline Neel

  • New Member
  • **
  • Posts: 5
  • Mole Snacks: +0/-0
Sulfoxide elimination
« on: April 03, 2012, 04:17:19 PM »
Hi, I tried the following reaction, but I only see starting material even after 6 hours. When I leave it overnight, compound degraded.

I would highly appreciate if you have any suggestions to make the product.


Offline sjb

  • Global Moderator
  • Sr. Member
  • ***
  • Posts: 3653
  • Mole Snacks: +222/-42
  • Gender: Male
Re: Sulfoxide elimination
« Reply #1 on: April 03, 2012, 04:44:18 PM »
Hi, I tried the following reaction, but I only see starting material even after 6 hours. When I leave it overnight, compound degraded.

I would highly appreciate if you have any suggestions to make the product.



Could you not make it from serine? Protect the nitrogen, esterify, oxidize the alcohol, methylenate, reduce?

What happens when you reduce the temperature? No reaction at all?

Offline Honclbrif

  • Chemist
  • Full Member
  • *
  • Posts: 659
  • Mole Snacks: +58/-10
  • Gender: Male
Re: Sulfoxide elimination
« Reply #2 on: April 03, 2012, 07:55:40 PM »
There could easily be a mass transport issue. How much CaCO3 are you using, and how finely powdered is it? Since the carbonate isn't soluble in your solvent, you're really only reacting on the surface of the particles, so you've got to stack the deck in your favor as much as you can. With that in mind, why not use use a phase transfer catalyst like TBAB, or K2CO3 and 18-crown-6?

You may also be able to do it with a selenoxide elimination instead.
Individual results may vary

Offline Neel

  • New Member
  • **
  • Posts: 5
  • Mole Snacks: +0/-0
Re: Sulfoxide elimination
« Reply #3 on: April 04, 2012, 07:09:55 PM »
Hi, I tried the following reaction, but I only see starting material even after 6 hours. When I leave it overnight, compound degraded.

I would highly appreciate if you have any suggestions to make the product.



Could you not make it from serine? Protect the nitrogen, esterify, oxidize the alcohol, methylenate, reduce?

What happens when you reduce the temperature? No reaction at all?

I tried the rxn at 150 C - still no rxn.

I have already done 3 steps, So would like to get this rxn going before thinking of alternate routes.

Thanks.

Offline Neel

  • New Member
  • **
  • Posts: 5
  • Mole Snacks: +0/-0
Re: Sulfoxide elimination
« Reply #4 on: April 04, 2012, 07:12:55 PM »
There could easily be a mass transport issue. How much CaCO3 are you using, and how finely powdered is it? Since the carbonate isn't soluble in your solvent, you're really only reacting on the surface of the particles, so you've got to stack the deck in your favor as much as you can. With that in mind, why not use use a phase transfer catalyst like TBAB, or K2CO3 and 18-crown-6?

You may also be able to do it with a selenoxide elimination instead.

I am using 2 molar eq. of a finely powdered CaCO3.

I will try TBAB.

Thanks.


Offline Honclbrif

  • Chemist
  • Full Member
  • *
  • Posts: 659
  • Mole Snacks: +58/-10
  • Gender: Male
Re: Sulfoxide elimination
« Reply #5 on: April 05, 2012, 12:10:59 PM »
If you're sticking with the calcium carbonate, I'd up it to more like 10 equivalents. Its cheap and should be relatively easy to separate by filtration there shouldn't be a big issue with using a large excess.
Individual results may vary

Offline Dan

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 4716
  • Mole Snacks: +469/-72
  • Gender: Male
  • Organic Chemist
    • My research
Re: Sulfoxide elimination
« Reply #6 on: April 06, 2012, 02:54:46 AM »
I can't see your scheme, but if you need a more soluble carbonate, try Cs2CO3 - it has slight solubility in organic solvents, dramatically reduces reaction times in comparison to, say, K2CO3 and without a massive molar excess.

I'm doing a lot of sulfinate eliminations at the moment, and 10 eq K2CO3 in THF at reflux takes 8-16 hours, whereas 2.5 eq  Cs2CO3 in refluxing THF takes 30-60 min.
My research: Google Scholar and Researchgate

Offline Neel

  • New Member
  • **
  • Posts: 5
  • Mole Snacks: +0/-0
Re: Sulfoxide elimination
« Reply #7 on: April 06, 2012, 11:31:25 PM »
If you're sticking with the calcium carbonate, I'd up it to more like 10 equivalents. Its cheap and should be relatively easy to separate by filtration there shouldn't be a big issue with using a large excess.

Thanks. I'll try.

Offline Neel

  • New Member
  • **
  • Posts: 5
  • Mole Snacks: +0/-0
Re: Sulfoxide elimination
« Reply #8 on: April 06, 2012, 11:32:15 PM »
I can't see your scheme, but if you need a more soluble carbonate, try Cs2CO3 - it has slight solubility in organic solvents, dramatically reduces reaction times in comparison to, say, K2CO3 and without a massive molar excess.

I'm doing a lot of sulfinate eliminations at the moment, and 10 eq K2CO3 in THF at reflux takes 8-16 hours, whereas 2.5 eq  Cs2CO3 in refluxing THF takes 30-60 min.

I'd try this option, too.

Sponsored Links