4'-Trifluoromethyl-biphenyl-3-carbaldehyde → 4'-(Trifluoromethyl)[1,1'-biphenyl]-3-methanol
Reaction equation
[BH4-].[Na+].[F:3][C:4]([F:20])([F:19])[C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH:17]=[O:18])[CH:12]=2)=[CH:7][CH:6]=1>>[F:3][C:4]([F:19])([F:20])[C:5]1[CH:6]=[CH:7][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][OH:18])[CH:12]=2)=[CH:9][CH:10]=1Participants
3
Procedure
The titled compound was prepared by standard NaBH4 reduction of 4′-trifluoromethyl-biphenyl-3-carbaldehyde (quant.). 1NMR (400 MHz, CDCl3) δ ppm: 7.40, 7.70 (m, 8H), 4.79 (s, 2H).
Sources & evidence
- ORD record
- ord-2440616816bf4890bf0fc85620416f97
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07989457B2
Reaction notes
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