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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003252Generated: October 30, 2026

Dimethyl Sulfoxide → (2S)-1-tert-butoxycarbonyl-2-phenylpiperidin-3-one

https://huagongshe.com/reaction/1003252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant(2S,3S)-1-t-Butyloxycarbonyl-3-hydroxy-2-phenylpiperidineHCID 10901890—
SolventDichloromethaneHCID 6344—
Product(2S)-1-tert-butoxycarbonyl-2-phenylpiperidin-3-oneHCID 10956740—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a cooled (-60° C.) solution of oxalyl chloride (0.68 ml, 7.8 mmol) in dichloromethane (17 ml) was added dimethyl sulfoxide (0.69 ml, 9.8 mmol) over 10 minutes before addition of (2S,3S)1-tert-butoxycarbonyl-3-hydroxy-2-phenylpiperidine (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 0° C. then was washed with ice cold 10% aqueous citric acid solution (40 ml, twice) water and dried (MgSO4). The solution was evaporated to dryness to give the title compound and this was used immediately without further purification. 1H NMR (250 MHz, CDCl3) δ 7.5-7.3 (5H,m), 5.8 (1H, bs), 4.2 (1H, bs), 3.4 (1H, m), 2.6 (2H, m), 2.0 (2H, m), 1.54 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046195
Source datasetuspto-grants-2000_04
ORD IDord-e64f50b7296d474ab7814b34de0041fc
Source noteuspto-grants-2000_04