3-Bromothiophene → 1-(3,5-Dimethyl-4-isoxazolyl)-1-(3-thienyl)ethanol
Reaction equation
[C:1]([C:4]1[C:5]([CH3:10])=[N:6][O:7][C:8]=1[CH3:9])(=[O:3])[CH3:2].Br[C:12]1[CH:16]=[CH:15][S:14][CH:13]=1>>[CH3:10][C:5]1[C:4]([C:1]([C:12]2[CH:16]=[CH:15][S:14][CH:13]=2)([OH:3])[CH3:2])=[C:8]([CH3:9])[O:7][N:6]=1Participants
3
Procedure
The title compound was prepared following the general method of Example 4 but starting with 4-acetyl-3,5-dimethylisoxazole and 3-bromothiophene. M.p. 93.5°-95° C.
Sources & evidence
- ORD record
- ord-73361ddd1a4d4dab8a837cb8a7040f81
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05607956
Reaction notes
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