HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Acetone → 2-Methoxy-4-phenylbenzoic acid

HRID 1470631
Notes
Print preview

Reaction equation

HRID 1470631 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:6]=[CH:7][C:8]=1[CH:9]=[O:10].CC(C)=[O:19]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:6]=[CH:7][C:8]=1[C:9]([OH:19])=[O:10]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 180AcetoneHCID 109658272-Methoxy-4-phenylbenzaldehyde

Product 1

HCID 186874072-Methoxy-4-phenylbenzoic acidYield 73.5%

Procedure

To a cold solution of 3-methoxy-biphenyl-4-carboxaldehyde (0.32 g, 1.5 mmol) in acetone (10 mL), the Jone's reagent was added slowly drop wise at 0° C. until the reaction completes. Acetone was removed completely and the resulting residue was diluted with water, extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over sodium sulphate and concentrated to obtain the title compound (0.25 g, 73.5%)

Workup

  1. customAcetone was removed completely
  2. additionthe resulting residue was diluted with water
  3. extractionextracted with ethyl acetate
  4. washThe combined organic layers were washed with water and brine
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • dry with materialdried over sodium sulphate
  • concentrationconcentrated
  • Sources & evidence

    ORD record
    ord-f375edc84d7847e68ba03792a09ca254
    Source dataset
    uspto-grants-2015_04
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US09006454B2

    Reaction notes

    Loading…