Sodium Hydroxide → HCID 10379653, compound
Reaction equation
[C:1]1([C:7]([CH:9]2[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:11][CH2:10]2)=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[OH-].[Na+]>C(Cl)Cl>[C:1]1([C:7]([CH:9]2[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:11][CH2:10]2)=[O:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Mix phenyl[1-(2-phenylethyl)-4-piperidinyl]methanone·HCl (5.0g, 15.16mmol), 1N sodium hydroxide (100mL) and methylene chloride (250mL) and stir overnight at room temperature. Separate the organic phase and extract the aqueous phase with methylene chloride. Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo to give phenyl[1-(2-phenylethyl)-4-piperidinyl]methanone.
Workup
- customSeparate the organic phase
- extractionextract the aqueous phase with methylene chloride
- dry with materialdry (MgSO4)
- customevaporate the solvent in vacuo
Sources & evidence
- ORD record
- ord-d9612964958141759866b83a38c87061
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05596003
Reaction notes
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