Hydride → HCID 53850202, compound
Reaction equation
[CH:1]1[C:11]2[CH:10]=[CH:9][C:8]3[CH:12]=[CH:13][CH:14]=[CH:15][C:7]=3[C:6](=[C:16]3[CH2:21][CH2:20][N:19]([C:22](=O)[CH:23]=[CH:24][C:25]4[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][C:26]=4[O:33][CH3:34])[CH2:18][CH2:17]3)[C:5]=2[CH:4]=[CH:3][CH:2]=1.[Li].[H-]>>[CH:12]1[C:8]2[CH:9]=[CH:10][C:11]3[CH:1]=[CH:2][CH:3]=[CH:4][C:5]=3[C:6](=[C:16]3[CH2:17][CH2:18][N:19]([CH2:22][CH:23]=[CH:24][C:25]4[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][C:26]=4[O:33][CH3:34])[CH2:20][CH2:21]3)[C:7]=2[CH:15]=[CH:14][CH:13]=1Participants
4
Procedure
4-(5H-Dibenzo[a,d]cyclohepten-5-ylidene)-1-(2,4-dimethoxycinnamoyl)piperidine was reduced with lithium alminium hydride. Yield 12.3%
Sources & evidence
- ORD record
- ord-a96cf5390bb04809965a5482a323e64e
- Source dataset
- uspto-grants-1993_07
- Patent number
- US05229400
Reaction notes
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