Diisobutylaluminum hydride → HCID 22557552, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5](/[C:8](/[CH3:16])=[C:9](\[CH3:15])/[C:10](OCC)=[O:11])=[CH:4][CH:3]=1.CC(C[AlH]CC(C)C)C>>[Br:1][C:2]1[CH:3]=[CH:4][C:5](/[C:8](/[CH3:16])=[C:9](\[CH3:15])/[CH2:10][OH:11])=[CH:6][CH:7]=1Participants
3
Procedure
(E)-Ethyl 3-(4-bromophenyl)-2-methyl-but-2-enoate (2.83 g, 9.99 mmol) was reduced with DIBAL-H by a procedure analogous to that described in example 52b to give (E)-3-(4-bromophenyl)-2-methyl-but-2-en-1-ol as a colourless oil; 1.82 g (75%).
Sources & evidence
- ORD record
- ord-5a4ae45d517b4ab58e771d5c69b9a1a4
- Source dataset
- uspto-grants-2005_03
- Patent number
- US06867218B2
Reaction notes
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