Acetic Acid → 5-Cyclopropylisoxazole-4-carboxylic acid
Reaction equation
[CH:1]1([C:4]2[O:8][N:7]=[CH:6][C:5]=2[C:9]([O:11]CC)=[O:10])[CH2:3][CH2:2]1.C(O)(=O)C.Cl>O>[CH:1]1([C:4]2[O:8][N:7]=[CH:6][C:5]=2[C:9]([OH:11])=[O:10])[CH2:2][CH2:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 5-cyclopropylisoxazole-4-carboxylate (203.0 g, 1.12 mole) [prepared in Step B] was added to a solution of 405 ml of glacial acetic acid plus 505 ml of 6N HCl and the mixture was heated in an oil bath at 105°-110° C. for 3 h. After 18 h at ambient temperature the thick mixture was diluted with water, cooled in an ice bath and filtered to give 140.8 g (82%) of the title acid. Recrystallization of an aliquot from acetonitrile gave an analytical sample, mp 163°-165° C.
Workup
- temperaturethe mixture was heated in an oil bath at 105°-110° C. for 3 h
- temperaturecooled in an ice bath
- filtrationfiltered
Sources & evidence
- ORD record
- ord-d30759c1d4f141d499fd3f47927a7dd4
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04935434
Reaction notes
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