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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265149Generated: October 30, 2026

Water → HCID 23157020, compound

https://huagongshe.com/reaction/2265149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroformHCID 6212—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantBenzyl 4-(2-chlorophenyl)-4-hydroxypiperidine-1-carboxylateHCID 23157061—
SolventEthyl AcetateHCID 8857—
ProductHCID 23157020HCID 23157020—

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a nitrogen atmosphere, 5.26 mL of diethylaminosulfur trifluoride was added to chloroform (160 mL) solution of 5.51 g of benzyl 4-(2-chlorophenyl)-4-hydroxypiperidine-1-carboxylate at −78° C., and stirred for 1 hour at −78° C. Water was added to the reaction liquid, and extracted with chloroform. The chloroform layer was dried with anhydrous sodium sulfate. The solvent was evaporated off under reduced pressure, and the residue was dissolved in 150 mL of acetone/water (2:1) mixture. 15.9 mL of aqueous 0.05 M osmium tetroxide solution and 3.73 g of N-methylmorpholine N-oxide were added thereto, and stirred overnight at room temperature. The reaction liquid was diluted with ethyl acetate, washed with aqueous sodium hydrogencarbonate solution, and dried with anhydrous sodium sulfate. The solvent was evaporated off under reduced pressure, and the residue was separated and purified through silica gel column chromatography (hexane/ethyl acetate=10/1) to obtain 2.11 g of the entitled compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855294B2
Source datasetuspto-grants-2010_12
ORD IDord-fac1cc0c4cf2407ebd80c37fb059d091
Source noteuspto-grants-2010_12