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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107274Generated: October 30, 2026

Dimethyl Sulfoxide → tert-Butyl 3-oxo-2-phenylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1107274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-t-Butyloxycarbonyl-3-hydroxy-2-phenylpiperidineHCID 21584093—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 3-oxo-2-phenylpiperidine-1-carboxylateHCID 11414684—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a cooled (-60° C.) solution of oxalyl chloride (0.68 ml, 7.8 mmol) in dichloronmethane (17 ml) was added dimethyl sulphoxide (0.69 ml, 9.8 mmol) for 10 minutes before addition of (±)1-tert-butoxycarbonyl-3-hydroxy-2-phenylpiperidine (1.8 g, 6.5 mmol; prepared by the method described in European Patent Specification number 0 528 495-A) in dichloromethane (7 ml). The solution was stirred at -60° C. for 20 minutes, warmed to -30° C. and triethylamine (2.5 ml) added. The solution was warmed to room temperature then was washed with ice cold 10% aqueous citric acid solution (40 ml, twice), water and dried (MgSO4). After evaporation the residue was purified by chromatography on silica gel (eluting with hexane containing an increasing proportion of ethyl acetate up to 20%) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060469
Source datasetuspto-grants-2000_05
ORD IDord-7bfb5fe95396445f8219e89207c58322
Source noteuspto-grants-2000_05