Diisobutylaluminum hydride → HCID 22557709, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:13]=[CH:12][C:11](/[C:14](/[CH3:19])=[CH:15]/[C:16]([O-])=[O:17])=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.CC(C[AlH]CC(C)C)C>>[CH3:1][C:2]1[CH:3]=[C:4]([C:8]2[CH:13]=[CH:12][C:11](/[C:14](/[CH3:19])=[CH:15]/[CH2:16][OH:17])=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
(E)-3-(3′-Methyl-biphenyl-4-yl)-but-2-enoate (0.74 g, 2.64 mmol) was reduced with DIBAL-H by a procedure analogous to that described in example 52b to give (E)-3-(3′-methyl-biphenyl-4-yl)-but-2-en-1-ol as a colourless solid; 0.63 g (85%).
Sources & evidence
- ORD record
- ord-3f5dc0bb2bcb4ce2bd4b0174fbc40de4
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06555577B1
Reaction notes
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