HCID 9907985, compound → HCID 9864968, compound
Reaction equation
[C:1]([O:4][C:5]1[CH:26]=[CH:25][C:8]([C:9]2[C:18](=[O:19])[C:17]3[C:12](=[C:13]([CH3:24])[C:14]([O:20][C:21](=[O:23])[CH3:22])=[CH:15][CH:16]=3)[O:11][CH:10]=2)=[CH:7][C:6]=1[O:27][CH3:28])(=[O:3])[CH3:2]>CO.[Pd]>[C:1]([O:4][C:5]1[CH:26]=[CH:25][C:8]([CH:9]2[CH:18]([OH:19])[C:17]3[C:12](=[C:13]([CH3:24])[C:14]([O:20][C:21](=[O:23])[CH3:22])=[CH:15][CH:16]=3)[O:11][CH2:10]2)=[CH:7][C:6]=1[O:27][CH3:28])(=[O:3])[CH3:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
4′,7-Diacetoxy-3′-methoxy-8-methylisoflavan-4-ol was prepared from 4′,7-diacetoxy-3′-methoxy-8-methylisoflavone (0.25 g, 0.7 mmol) in methanol (50 ml) using palladium-on-charcoal (5%, 0.07 g) by the method described above.
Sources & evidence
- ORD record
- ord-d386049ed7754ec89a0c66917712f44f
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07906660B2
Reaction notes
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