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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620604Generated: October 31, 2026

Dimethyl Sulfoxide → 1-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carbaldehyde

https://huagongshe.com/reaction/1620604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
Reactant1-[2,4-Bis(trifluoromethyl)benzyl]-4-(hydroxymethyl)piperidin-2-oneHCID 86678774—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product1-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carbaldehydeHCID 8667877537.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of oxalyl chloride (4.5 mL) in dichloromethane (80 mL) was added a solution of dimethyl sulfoxide (7.3 mL) in dichloromethane (50 mL) under cooling to −78° C. The reaction mixture was stirred for 30 min under cooling to −78° C., and to the reaction mixture was added dropwise a solution of 1-[2,4-bis(trifluoromethyl)benzyl]-4-(hydroxymethyl)piperidin-2-one (10 g) in dichloromethane (50 mL). The reaction mixture was stirred for 40 min under cooling to −78° C., triethylamine (19.7 mL) was added, and the mixture was further stirred at room temperature for 30 min. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with dichloromethane. The extract was washed with saturated brine, dried over sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/petroleum ether) to give the title compound (3.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-94bb054148b7426c864346f923180f6f
Source noteuspto-grants-2014_07