Ethanol → 2-(2-Methoxyphenyl)-2-oxoacetaldehyde

HRID 34736Notes

Reaction equation

HRID 34736 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9](=[O:11])[CH3:10].C([OH:14])C>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]([CH:10]=[O:14])=[O:11]

Participants

3

Procedure

SeO2 (12.4 g., 0.112 mol) was dissolved in 75 ml. of 95% ethanol by warming to 55°. o-Methoxyacetophenone (15.3 g., 0.102 mol) was added in one portion and the mixture refluxed 21 hours. The reaction mixture was treated with activated carbon, filtered over diatomaceous earth, and the filtrate stripped to yield to an oil, 23.2 g. The latter was distilled to yield purified title product, 8.4 g., bp 94°-96°/0.5 mm, which solidified on cooling.

Workup

  1. temperaturethe mixture refluxed 21 hours
  2. additionThe reaction mixture was treated with activated carbon
  3. filtrationfiltered over diatomaceous earth
  4. customto yield to an oil, 23.2 g
  5. distillationThe latter was distilled
  6. customto yield
  7. custompurified title product, 8.4 g
  8. temperatureon cooling

Sources & evidence

ORD record
ord-48f8d9c6e4794a009e46c4eff477dccf
Source dataset
uspto-grants-1988_08
Patent number
US04762921

Reaction notes

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