Sodium borohydride → HCID 21707639, compound
Reaction equation
[BH4-].[Na+].[CH3:3][C:4]1([C:16](=[O:18])[CH3:17])[CH2:6][CH:5]1[CH2:7][CH:8]1[CH2:12][CH:11]=[C:10]([CH3:13])[C:9]1([CH3:15])[CH3:14]>>[CH3:3][C:4]1([CH:16]([OH:18])[CH3:17])[CH2:6][CH:5]1[CH2:7][CH:8]1[CH2:12][CH:11]=[C:10]([CH3:13])[C:9]1([CH3:15])[CH3:14]Participants
3
Procedure
Sodium borohydride reduction of 3.0 g (13.6 mmol) of 1-[1-methyl-2-(2,2,3-trimethyl-cyclopent-3-enylmethyl)cyclopropyl]ethanone from Example 12a according to Example 1b gave 1.6 g of 1-[1-methyl-2-(2,2,3-trimethylcyclopent-3-enylmethyl)cyclopropyl]ethanol (53% yield).
Sources & evidence
- ORD record
- ord-18f83bcd0ec9459cace77b4be6501b26
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06239314B1
Reaction notes
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