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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606154Generated: October 25, 2026

Dimethyl Sulfoxide → 1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanone

https://huagongshe.com/reaction/606154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanolHCID 22248173—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanoneHCID 2224799373%

Reaction Conditions

Temperature-78 °C

Reaction Steps

After dissolving 7.5 ml of oxalyl chloride in 130 ml of dichloromethane, the solution was cooled to −78° C. and a solution of 6.1 ml of dimethylsulfoxide in dichloromethane (20 ml) was added dropwise while stirring. After stirring for 20 minutes, a solution of 13.4 g of 1-(1-benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanol in dichloromethane (40 ml) was added dropwise. After stirring for 30 minutes, 24 ml of triethylamine was added and the temperature was raised to room temperature. Water was added to the reaction solution, the organic layer was washed with water and saturated brine in that order and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by NH silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (9.64 g, 73% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915274B2
Source datasetuspto-grants-2011_03
ORD IDord-722ea4779f1247ca9b73bbff3e9331fa
Source noteuspto-grants-2011_03