Diisobutylaluminum hydride → (E)-3-(2'-methyl-biphenyl-4-yl)-but-2-en-1-ol
Reaction equation
CC(C[AlH]CC(C)C)C.[CH3:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[C:17]1[CH:22]=[CH:21][C:20](/[C:23](/[CH3:30])=[CH:24]/[C:25](OCC)=[O:26])=[CH:19][CH:18]=1>>[CH3:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[C:17]1[CH:18]=[CH:19][C:20](/[C:23](/[CH3:30])=[CH:24]/[CH2:25][OH:26])=[CH:21][CH:22]=1Participants
3
Procedure
The colourless oil (E)-3-(2′-methyl-biphenyl-4-yl)-but-2-en-1-ol was prepared by DIBAL-H reduction of (E)-ethyl 3-(2′-methyl-biphenyl-4-yl)-but-2-enoate by a procedure analogous to that described in example 50b.
Sources & evidence
- ORD record
- ord-41bc202b34404362b88808e0356c3410
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06867218B2
Reaction notes
Loading…