Methyl 4-(1,3-oxazol-5-yl)benzoate → 4-(1,3-Oxazol-5-yl)benzoic Acid
Reaction equation
[O:1]1[C:5]([C:6]2[CH:15]=[CH:14][C:9]([C:10]([O:12]C)=[O:11])=[CH:8][CH:7]=2)=[CH:4][N:3]=[CH:2]1>[OH-].[K+].C1COCC1>[O:1]1[C:5]([C:6]2[CH:7]=[CH:8][C:9]([C:10]([OH:12])=[O:11])=[CH:14][CH:15]=2)=[CH:4][N:3]=[CH:2]1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The above ester was heated at reflux for 2 hours in a mixture of 1 M aqueous potassium hydroxide and 50 ml THF. The THF was removed in vacuo and the solution cooled, then acidified with 50% HCl to give 4-(1,3-oxazol-5-yl)benzoic acid as a white solid.
Workup
- customThe THF was removed in vacuo
- temperaturethe solution cooled
Sources & evidence
- ORD record
- ord-0a5af2004eb4411f8299c78bf38fbeac
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07425557B2
Reaction notes
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