Diisobutylaluminum hydride → HCID 22557582, compound
Reaction equation
CC(C[AlH]CC(C)C)C.[C:10]1([C:16]2[CH:21]=[C:20](/[CH:22]=[CH:23]/[C:24](OCC)=[O:25])[CH:19]=[C:18]([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[CH:17]=2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[C:10]1([C:16]2[CH:21]=[C:20](/[CH:22]=[CH:23]/[CH2:24][OH:25])[CH:19]=[C:18]([C:29]3[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=3)[CH:17]=2)[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
3
Procedure
The colourless solid (E)-3-[1,1′;3′,1″]terphenyl-5′-yl-prop-2-en-1-ol was prepared by DIBAL-H reduction of (E)-ethyl 3-[1,1′;3′,1″]terphenyl-5′-yl-acrylate by a procedure analogous to that described for example 52b.
Sources & evidence
- ORD record
- ord-1c8d99c3ef5b4877b0f7bb15ddc0a586
- Source dataset
- uspto-grants-2003_04
- Patent number
- US06555577B1
Reaction notes
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