1-Acetyl-4-(2',4'-difluorobenzoyl)piperidine → (2,4-Difluorophenyl)(piperidin-4-yl)methanone
Reaction equation
C([N:4]1[CH2:9][CH2:8][CH:7]([C:10](=[O:19])[C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][C:12]=2[F:18])[CH2:6][CH2:5]1)(=O)C>Cl>[F:18][C:12]1[CH:13]=[C:14]([F:17])[CH:15]=[CH:16][C:11]=1[C:10]([CH:7]1[CH2:6][CH2:5][NH:4][CH2:9][CH2:8]1)=[O:19]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
30 g of 1-acetyl-4-(2,4-difluorobenzoyl)piperidine are brought to reflux in 113 ml of 6N hydrochloric acid for 6 hours. The reaction medium is then concentrated and the residue obtained is crystallized in isopropanol. The expected compound is isolated after filtration.
Workup
- concentrationThe reaction medium is then concentrated
- customthe residue obtained
- customis crystallized in isopropanol
Sources & evidence
- ORD record
- ord-5a5424fd76de439ea27c974720c1127d
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05100902
Reaction notes
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