Hydrofluoric Acid → HCID 131718000, compound
Reaction equation
F.[O:2]([CH:10]([C:31]([F:36])([F:35])[CH2:32][CH2:33][CH3:34])[CH2:11][CH2:12][CH2:13][C@H:14]1[C@H:18]([CH3:19])[CH2:17][C:16](=[O:20])[C@@H:15]1[CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH2:26][C:27]([O:29][CH3:30])=[O:28])[Si](C(C)(C)C)(C)C>C(#N)C>[OH:2][CH:10]([C:31]([F:35])([F:36])[CH2:32][CH2:33][CH3:34])[CH2:11][CH2:12][CH2:13][C@H:14]1[C@H:18]([CH3:19])[CH2:17][C:16](=[O:20])[C@@H:15]1[CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH2:26][C:27]([O:29][CH3:30])=[O:28]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrofluoric acid (1 ml) was added to a solution of the compound (30) (0.201 g) in acetonitrile (20 ml). The resultant mixture was stirred at room temperature for 1 hour. The crude product obtained after the usual work-up was subjected to silicagel column chromatography to give the alcohol (31).
Workup
- customThe crude product obtained after the usual work-up
Sources & evidence
- ORD record
- ord-bfa113902e8649d09b84875394ef4c53
- Source dataset
- uspto-grants-1993_06
- Patent number
- US05221799
Reaction notes
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