Diisobutylaluminum hydride → (E)-3-(3',5'-dichloro-biphenyl-4-yl)-but-2-en-1-ol
Reaction equation
CC(C[AlH]CC(C)C)C.[Cl:10][C:11]1[CH:12]=[C:13]([C:18]2[CH:23]=[CH:22][C:21](/[C:24](/[CH3:31])=[CH:25]/[C:26](OCC)=[O:27])=[CH:20][CH:19]=2)[CH:14]=[C:15]([Cl:17])[CH:16]=1>>[Cl:10][C:11]1[CH:12]=[C:13]([C:18]2[CH:19]=[CH:20][C:21](/[C:24](/[CH3:31])=[CH:25]/[CH2:26][OH:27])=[CH:22][CH:23]=2)[CH:14]=[C:15]([Cl:17])[CH:16]=1Participants
3
Procedure
The colourless oil (E)-3-(3′,5′-dichloro-biphenyl-4-yl)-but-2-en-1-ol was prepared by DIBAL-H reduction of (E)-ethyl 3-(3′,5′-dichloro-biphenyl-4-yl)-but-2-enoate as described for example 52b.
Sources & evidence
- ORD record
- ord-b6ccab1ea75b4a36808ffa62f245a9dc
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06867218B2
Reaction notes
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