September 21, 2024, 01:37:38 AM
Forum Rules: Read This Before Posting


Topic: Finkelstein Reaction  (Read 1897 times)

0 Members and 1 Guest are viewing this topic.

Offline AlphaScent

  • Full Member
  • ****
  • Posts: 638
  • Mole Snacks: +24/-7
  • Gender: Male
Finkelstein Reaction
« on: May 08, 2013, 07:27:54 PM »
Hey all,

Does anyone have a finkelstein procedure available to them with the intermediate being a tosylate??

Thank you so much!

Cheers
If you're not part of the solution, then you're part of the precipitate

Offline AlphaScent

  • Full Member
  • ****
  • Posts: 638
  • Mole Snacks: +24/-7
  • Gender: Male
If you're not part of the solution, then you're part of the precipitate

Offline discodermolide

  • Chemist
  • Sr. Member
  • *
  • Posts: 5038
  • Mole Snacks: +405/-70
  • Gender: Male
    • My research history
Re: Finkelstein Reaction
« Reply #2 on: May 08, 2013, 09:10:41 PM »
Don't see why you can't use the original procedure given here with a chloride.
http://orgsyn.org/orgsyn/default.asp?formgroup=basenpe_form_group&dataaction=db&dbname=orgsyn
« Last Edit: May 08, 2013, 09:56:18 PM by discodermolide »
Development Chemists do it on Scale, Research Chemists just do it!
My Research History

Sponsored Links