1-(4-Phenylbutoxy)hept-6-en-3-ol → 1-(4-Phenylbutoxy)hept-6-en-3-one
Reaction equation
[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][CH:14]([OH:19])[CH2:15][CH2:16][CH:17]=[CH2:18])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(CCCCOCCC=O)C=CC=CC=1>>[C:1]1([CH2:7][CH2:8][CH2:9][CH2:10][O:11][CH2:12][CH2:13][C:14](=[O:19])[CH2:15][CH2:16][CH:17]=[CH2:18])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
Obtained from Intermediate 14 (0.41 g, 1.56 mmol) by the procedure described for the Intermediate 13. Purification by column chromatography with silica gel and methylene chloride/acetone (20:1) as eluent gave the title compound (0.36 g, 88%) as oil.
Workup
- customPurification by column chromatography with silica gel and methylene chloride/acetone (20:1) as eluent
Sources & evidence
- ORD record
- ord-3833f2ff588146258ed464e519f79028
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08242177B2
Reaction notes
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