Sodium borohydride → HCID 57890118, compound
Reaction equation
[CH2:1]([C:3]([C:12]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][C:20](=[O:25])[C:21]([CH3:24])([CH3:23])[CH3:22])=[C:14]([CH3:26])[CH:13]=1)([C:6]1[S:7][CH:8]=[C:9]([CH3:11])[CH:10]=1)[CH2:4][CH3:5])[CH3:2].[BH4-].[Na+]>>[CH2:1]([C:3]([C:12]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][CH:20]([OH:25])[C:21]([CH3:24])([CH3:23])[CH3:22])=[C:14]([CH3:26])[CH:13]=1)([C:6]1[S:7][CH:8]=[C:9]([CH3:11])[CH:10]=1)[CH2:4][CH3:5])[CH3:2]Participants
3
Procedure
Using a procedure analogous to Example 134B, 1-{4-[1-ethyl-1-(4-methyl-thiophen-2-yl)-propyl]-2-methyl-phenyl}-4,4-dimethyl-pentan-3-one and NaBH4 give the title compound (quant).
Sources & evidence
- ORD record
- ord-3bd294d6f3664340af5f06e8fddc7889
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07601850B2
Reaction notes
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