April 27, 2024, 02:13:42 PM
Forum Rules: Read This Before Posting


« previous next »
Pages: [1]   Go Down

Topic: grignard reagent out of alcohols  (Read 2513 times)

0 Members and 1 Guest are viewing this topic.

Offline asd5110

  • New Member
  • **
  • Posts: 4
  • Mole Snacks: +0/-0
grignard reagent out of alcohols
« on: December 17, 2010, 03:40:25 AM »
why cant you make grignard reagents out of alcholos? i understand that you can convert the OH group to a Br using PBr3 in ether and carry on from there. i just wanted to why its not possible
Logged

Offline Hybrid

  • Regular Member
  • ***
  • Posts: 63
  • Mole Snacks: +3/-3
Re: grignard reagent out of alcohols
« Reply #1 on: December 17, 2010, 05:08:52 AM »
let me get it , u mean RMgOH instead of RMgBr or RMgBr from ROH
Logged

Offline discodermolide

  • Chemist
  • Sr. Member
  • *
  • Posts: 5038
  • Mole Snacks: +405/-70
  • Gender: Male
    • My research history
Re: grignard reagent out of alcohols
« Reply #2 on: December 18, 2010, 12:28:31 PM »
Quote from: asd5110 on December 17, 2010, 03:40:25 AM
why cant you make grignard reagents out of alcholos? i understand that you can convert the OH group to a Br using PBr3 in ether and carry on from there. i just wanted to why its not possible

You will generate a Magnesium alkoxide not a Grignard reagent. For that you usually require a halide.
Logged
Development Chemists do it on Scale, Research Chemists just do it!
My Research History
Pages: [1]   Go Up
« previous next »
Sponsored Links