June 01, 2020, 10:35:18 AM
Forum Rules: Read This Before Posting

Topic: protection of the carbonyl of an enone  (Read 3471 times)

0 Members and 1 Guest are viewing this topic.

Offline g-bones

  • Chemist
  • Full Member
  • *
  • Posts: 197
  • Mole Snacks: +22/-7
protection of the carbonyl of an enone
« on: August 28, 2009, 04:38:22 PM »
I am reviewing some problems and I have the attached problem in which i am given the starting material and the reagents and must predict the product.  when I first looked at it I didn't think much and came up with the reaction path and the product shown.  the only thing I am worried about is whether the formation of the acetal will be productive or whether a michael addition would occur instead thus destroying the double bond and not giving the ozone anything to react with.  anybody have any thoughts.

Offline Arctic-Nation

  • Chemist
  • Full Member
  • *
  • Posts: 265
  • Mole Snacks: +33/-9
Re: protection of the carbonyl of an enone
« Reply #1 on: August 30, 2009, 04:45:18 PM »
I don't really expect any problems. Some side reactions might occur, but oxygen loves hard-hard interactions, so glycol addition should only happen at the carbonyl-carbon, not at the beta-position.

Sponsored Links