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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862199Generated: October 26, 2026

Dimethyl Sulfoxide → 1-(3-Methoxyphenyl)-2-pyridin-4-ylethane-1,2-dione

https://huagongshe.com/reaction/862199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(3-Methoxyphenyl)-2-pyridin-4-ylethane-1,2-diolHCID 18704770—
SolventDichloromethaneHCID 6344—
Product1-(3-Methoxyphenyl)-2-pyridin-4-ylethane-1,2-dioneHCID 1870476062.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of methyl sulfoxide (11.8 g, 10.7 mL, 150 mmol) in dichloromethane (150 mL) at -78° C. was added trifluoroacetic anhydride (23.7 g, 16 mL, 113 mmol) dropwise. After ten minutes, 1-(3-methoxyphenyl)-2-pyridin-4-ylethane-1,2-diol (8.5 g, 34 mmol) in dichloromethane (60 mL) was added dropwise. After another ten minutes, triethylamine (21.3 g, 29.4 mL, 211 mmol) was added dropwise and the reaction mixture was immediately warmed to 0° C. and poured into saturated aqueous sodium hydrogen carbonate solution (300 mL). The aqueous layer was extracted with ethyl acetate (3×200 mL) and the organic layers were combined, dried over anhydrous magnesium sulfate and concentrated at reduced pressure. The resulting oil was chromatographed on silica gel eluting with 1:3 ethyl acetate:hexane to give the dione as a yellow solid (5.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05717100
Source datasetuspto-grants-1998_02
ORD IDord-1ff64f2b09984fcdad44407e63bd6648
Source noteuspto-grants-1998_02