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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584185Generated: October 31, 2026

Dimethyl Sulfoxide → (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-[2-(formylmethoxy)ethyl]piperazine

https://huagongshe.com/reaction/584185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
Reactant(2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-[2-(2-hydroxyethoxy)ethyl]piperazineHCID 86588510—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product(2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-[2-(formylmethoxy)ethyl]piperazineHCID 8658851154.1%

Reaction Conditions

Temperature-45 °C

Reaction Steps

To a stirred solution of oxalyl chloride (151 mg) in dichloromethane (3 ml) was added dropwise a solution of dimethylsulfoxide (123 mg) in dichloromethane (0.25 ml) at −78° C. under nitrogen atmosphere. After 15 minutes, (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-[2-(2-hydroxyethoxy)ethyl]piperazine (317 mg) was added at the same temperature. After 15 minutes, the resulting mixture was stirred at −45° C. for 1 hour. Triethylamine (446 mg) was added at −45° C., and the whole was stirred at 0° C. for 20 minutes and then treated with aqueous solution of ammonium chloride (2 ml). The organic layer was separated and dried over magnesium sulfate. After evaporation of the solvent, the resulting residue was purified by column chromatography on silica gel using ethyl acetate as eluent to afford (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-[2-(formylmethoxy)ethyl]piperazine (171 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-7a9a750feb5841668c085edf57e4a09e
Source noteuspto-grants-2005_08