November 22, 2024, 04:16:56 PM
Forum Rules: Read This Before Posting


Topic: Chromatography of an Aldehyde  (Read 3437 times)

0 Members and 1 Guest are viewing this topic.

Offline MasterChief

  • Regular Member
  • ***
  • Posts: 10
  • Mole Snacks: +0/-0
Chromatography of an Aldehyde
« on: November 19, 2012, 03:45:02 PM »
I have an aldehyde compound I need to run through a column. If I use MeOH (~4%) will I get some acetal as a side product?

Offline Dan

  • Retired Staff
  • Sr. Member
  • *
  • Posts: 4716
  • Mole Snacks: +469/-72
  • Gender: Male
  • Organic Chemist
    • My research
Re: Chromatography of an Aldehyde
« Reply #1 on: November 19, 2012, 06:30:05 PM »
I doubt it very much, at least not to an appreciable extent. If you could make acetals from aldehydes with just MeOH and silica, people would use it to make acetals when they wanted acetals. I may be wrong though. There is only one way to find out for sure with your aldehyde.

You could also consider alternative alcoholic eluents (e.g. IPA), or polar non-alcoholic eluents.

My research: Google Scholar and Researchgate

Offline mamid

  • Regular Member
  • ***
  • Posts: 30
  • Mole Snacks: +5/-1
Re: Chromatography of an Aldehyde
« Reply #2 on: November 22, 2012, 08:07:25 AM »
If your aldehyde doesn't contain other very polar groups like OH, COOH or NH2, you probably can use non-alcohol-containing solvents for elution.

Offline zhangcarlin

  • Regular Member
  • ***
  • Posts: 19
  • Mole Snacks: +0/-0
Re: Chromatography of an Aldehyde
« Reply #3 on: November 22, 2012, 09:25:04 AM »
Very likely. a mixture of ethyl acetate and THF can replace your eluent, if you are using DCM/MeOH

Sponsored Links