Diisobutylaluminum hydride → HCID 69796166, compound
Reaction equation
CC(C[AlH]CC(C)C)C.[C:10]([C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:25]=[CH:24][C:23](/[C:26](/[CH3:33])=[CH:27]/[C:28](OCC)=[O:29])=[CH:22][CH:21]=2)=[CH:16][CH:15]=1)([CH3:13])([CH3:12])[CH3:11]>>[C:10]([C:14]1[CH:19]=[CH:18][C:17]([C:20]2[CH:21]=[CH:22][C:23](/[C:26](/[CH3:33])=[CH:27]/[CH2:28][OH:29])=[CH:24][CH:25]=2)=[CH:16][CH:15]=1)([CH3:13])([CH3:11])[CH3:12]Participants
3
Procedure
The colourless gum (E)-3-(4′-tert-butyl-biphenyl-4-yl)-but-2-en-1-ol was prepared by DIBAL-H reduction of (E)-ethyl 3-(4′-tert-butyl-biphenyl-4-yl)-but-2-enoate by a procedure analogous to that described in example 52b.
Sources & evidence
- ORD record
- ord-a016418a28104229a29d363597234657
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06555577B1
Reaction notes
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