Methyl 3-phenyl-4-isoxazolecarboxylate → (3-Phenyl-1,2-oxazol-4-yl)methanol
Reaction equation
C[O:2][C:3]([C:5]1[C:6]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[N:7][O:8][CH:9]=1)=O.C(OC(C1C(C2C=CC=CC=2F)=NOC=1C)=O)C>>[C:10]1([C:6]2[C:5]([CH2:3][OH:2])=[CH:9][O:8][N:7]=2)[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
3
Procedure
As described for example 84d, 3-phenyl-isoxazole-4-carboxylic acid methyl ester (2.95 g, 15 mmol) was converted, instead of 3-(2-fluoro-phenyl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester, to the title compound (1.56 g, 61%) which was obtained as a light green oil. MS: m/e=176.4 [M+H]+.
Sources & evidence
- ORD record
- ord-61331c6062df48beb9a41e7dec6d7d16
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08846719B2
Reaction notes
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