Benzyl 4-(5-chloro-2-methoxyphenyl)piperidine-1-carboxylate → HCID 49760816, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:24][CH3:25])=[C:6]([CH:8]2[CH2:13][CH2:12][N:11](C(OCC3C=CC=CC=3)=O)[CH2:10][CH2:9]2)[CH:7]=1>Cl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:24][CH3:25])=[C:6]([CH:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[CH:7]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of benzyl 4-(5-chloro-2-methoxyphenyl)piperidine-1-carboxylate (Preparation 234, 73 g, 0.2 mol) in concentrated hydrochloric acid (200 ml) was refluxed with stirring for 2 hours before concentrating in vacuo. Water (100 ml), sodium hydroxide (10 M aqueous solution, 20 ml) and chloroform (200 ml) were added to the residue. The aqueous layer was extracted with chloroform (2×200 ml). The combined organic layers were washed with water (200 ml), saturated aqueous sodium chloride solution (200 ml), dried over sodium sulphate, filtered through silica gel (100 g, 40/63 μm) and evaporated in vacuo to afford the title compound as white crystals, 40 g, 89% yield.
Workup
- concentrationbefore concentrating in vacuo
- additionWater (100 ml), sodium hydroxide (10 M aqueous solution, 20 ml) and chloroform (200 ml) were added to the residue
- extractionThe aqueous layer was extracted with chloroform (2×200 ml)
- washThe combined organic layers were washed with water (200 ml), saturated aqueous sodium chloride solution (200 ml)
- dry with materialdried over sodium sulphate
- filtrationfiltered through silica gel (100 g, 40/63 μm)
- customevaporated in vacuo
Sources & evidence
- ORD record
- ord-79bc94f07bb143d7816d7be7b9eaa631
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08153814B2
Reaction notes
Loading…