3-(5-Methyl-1,2-oxazol-3-yl)propan-1-ol → 3-(5-Hydroxypentyl)-5-methylisoxazole
Reaction equation
[C:1]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]1(C)[CH:12]=[CH:11][O:10][NH:9]1)([OH:3])=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:20]C1ON=C(CCCO)C=1>>[OH:3][CH2:1][CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:12]=[C:11]([CH3:20])[O:10][N:9]=1Participants
4
Procedure
3-(5-Hydroxypentyl)-5-methylisoxazole was prepared by reduction of 3-(4-carboxybutyl)-3-methylisoxazole with lithium aluminum hydride according to the procedure of part (e) above, and was obtained in 84% yield as an oil, b.p. 115°-125° C. (0.1 mm).
Workup
- customwas obtained in 84% yield as an oil, b.p. 115°-125° C. (0.1 mm)
Sources & evidence
- ORD record
- ord-be238e1b44ec48ae83998c058606e6bc
- Source dataset
- uspto-grants-1991_03
- Patent number
- US05002960
Reaction notes
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