HCID 67785161, compound → HCID 19883664, compound
Reaction equation
[CH3:1][N:2]([CH3:24])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]/[CH:8]=[CH:9]\[C:10]1[CH:23]=[CH:22][C:13]([C:14]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[O:15])=[CH:12][CH:11]=1>CO.[Pd]>[CH3:24][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[CH:11]=[CH:12][C:13]([C:14]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[O:15])=[CH:22][CH:23]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
1.12 g of 4-[(Z)-7-(dimethylamino)-1-heptenyl]benzophenone were dissolved in 30 ml of methanol, 20 mg of 5 percent palladium on carbon were added thereto and the suspension was stirred under hydrogen at normal pressure and room temperature for 2.5 hours. The reaction mixture was filtered through silica gel and the filtrate was evaporated. There were obtained 1.10 g (98%) of 4-[7-(dimethylamino)heptyl]benzophenone as a colourless oil.
Workup
- filtrationThe reaction mixture was filtered through silica gel
- customthe filtrate was evaporated
Sources & evidence
- ORD record
- ord-0a5f69f9f57f428b8c3002107006fb42
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05137920
Reaction notes
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