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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754906Generated: October 28, 2026

Potassium Nitrate → 2-(4-Dimethylcarbamoyl-2-methyl-phenyl)-ethanesulfonyl chloride

https://huagongshe.com/reaction/1754906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
ReactantSulfuryl chlorideHCID 24648—
Reactant4-(2-mercapto-ethyl)-3,N,N-trimethyl-benzamideHCID 86672759—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product2-(4-Dimethylcarbamoyl-2-methyl-phenyl)-ethanesulfonyl chlorideHCID 8667276074%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Potassium nitrate (583 mg, 5.77 mmol) was added to a solution of 4-(2-mercapto-ethyl)-3,N,N-trimethyl-benzamide (514 mg, 2.30 mmol) in MeCN (23 ml) at room temperature. The mixture was cooled to −40° C., and sulfuryl chloride (1.68 M solution in dichloromethane, 3.46 ml, 5.81 mmol) was then added dropwise over 15 minutes. After stirring at −40° C. to −20° C. for 2.5 hours, the reaction mixture was diluted with dichloromethane (80 ml) and quenched with a saturated aqueous sodium bicarbonate solution (20 ml). The organic layer and the aqueous layer were separated, and the organic layer was then washed with a saturated aqueous sodium chloride solution (30 ml), dried over MgSO4 and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1→1/2) to give 2-(4-dimethylcarbamoyl-2-methyl-phenyl)-ethanesulfonyl chloride as a colorless solid (491 mg, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-3a8967aa22264254b5822a79ad3c84ac
Source noteuspto-grants-2015_10