HCID 9847690, compound → [2-(4-Methoxyphenyl)-6-methoxybenzofuran-3-yl][4-(2-diethylaminoethoxy]phenyl]methanol
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:10][C:11]3[CH:33]=[C:32]([O:34][CH3:35])[CH:31]=[CH:30][C:12]=3[C:13]=2[C:14]([C:16]2[CH:21]=[CH:20][C:19]([O:22][CH2:23][CH2:24][N:25]([CH2:28][CH3:29])[CH2:26][CH3:27])=[CH:18][CH:17]=2)=[O:15])=[CH:5][CH:4]=1>CO>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[O:10][C:11]3[CH:33]=[C:32]([O:34][CH3:35])[CH:31]=[CH:30][C:12]=3[C:13]=2[CH:14]([C:16]2[CH:21]=[CH:20][C:19]([O:22][CH2:23][CH2:24][N:25]([CH2:26][CH3:27])[CH2:28][CH3:29])=[CH:18][CH:17]=2)[OH:15])=[CH:7][CH:8]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
1.420 g (3 mmol) of [2-(4-methoxyphenyl)-6-methoxybenzofuran-3-yl][4-[2-diethylaminoethoxy]phenyl]methanone was reduced to the carbinol by the method described in Example 1. This yielded 1.07 g of the title compound as an oil.
Sources & evidence
- ORD record
- ord-29551e08d1554c74a87b1297b3f5ed77
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06407243B1
Reaction notes
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