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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862197Generated: October 29, 2026

Dimethyl Sulfoxide → 3,4-Dichlorophenyl-2-piperdin-4-yl-ethane-1,2-dione

https://huagongshe.com/reaction/862197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(3,4-Dichlorophenyl)-2-pyridin-4-yl-ethane-1,2-diolHCID 22185450—
SolventDichloromethaneHCID 6344—
Product3,4-Dichlorophenyl-2-piperdin-4-yl-ethane-1,2-dioneHCID 13172046771.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of methyl sulfoxide (38.3 g, 35 mL, 490 mmol) in dichloromethane (750 mL) at -78° C. was added trifluoroacetic anhydride (77 g, 52 mL, 368 mmol) dropwise. After ten minutes, 1-(3,4-dichlorophenyl)-2-pyridin-4-yl-ethane-1,2-diol (31.7 g, 112 mmol) in dichloromethane (500 mL) was added dropwise. After another ten minutes, triethylamine (70 g, 96 mL, 690 mmol) was added dropwise and the reaction mixture immediately warmed to 0° C. and poured into saturated aqueous sodium hydrogen carbonate (300 mL). The aqueous layer was extracted with ethyl acetate (3×200 mL) and the organic layers were combined, dried over anhydrous magnesium sulfate, filtered and concentrated at reduced pressure. The resulting solid was triturated with ethyl acetate to give the dione as a yellow solid (23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05717100
Source datasetuspto-grants-1998_02
ORD IDord-a256b20682034e6fa6cd678107f0f0bf
Source noteuspto-grants-1998_02