Water → Ethyl 4-(piperidin-1-yl)benzoate
Reaction equation
F[C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][CH:3]=1.[NH:13]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.O>C(#N)C>[N:13]1([C:2]2[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][CH:3]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Reaction of ethyl 4-fluorobenzoate with piperidine (3 equivalents) in acetonitrile may be carried out at reflux for 4 days. Dilution of the cooled reaction mixture with several volumes of water provides a precipitate, which may be filtered to provide ethyl 4-(piperidin-1-yl)benzoate. Reduction of the ester with lithium aluminum hydride (2 equivalents) in tetrahydrofuran provides the corresponding alcohol.
Workup
- temperatureat reflux for 4 days
- customprovides a precipitate, which
- filtrationmay be filtered
Sources & evidence
- ORD record
- ord-6cb6799b4a764d3fac9df5a1d191f153
- Source dataset
- uspto-grants-2002_01
- Patent number
- US06342497B1
Reaction notes
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