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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644765Generated: October 27, 2026

Sodium Thiosulfate → 4-{[4-(Methylsulfonyl)-1,3-thiazol-2-yl]carbamoyl}phenyl acetate

https://huagongshe.com/reaction/1644765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-{[4-(Methylthio)-1,3-thiazol-2-yl]carbamoyl}phenyl acetateHCID 57571887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-{[4-(Methylsulfonyl)-1,3-thiazol-2-yl]carbamoyl}phenyl acetateHCID 2518693530%

Reaction Steps

A solution of m-chloroperbenzoic acid (1.0 g, 6.0 mmol, maximum 77%) dissolved in dichloromethane (30 mL) was added to a suspension of 82 (0.63 g, 2.0 mmol) in dichloromethane (60 mL). The reaction became homogeneous and the dark brown solution became lighter with time. After 1.25 hours, saturated aqueous sodium thiosulfate was added to the reaction and the reaction mixture was stirred vigorously for 20 minutes. The yellow mixture was diluted with water and the resulting layers separated. The organic layer was washed twice with saturated aqueous sodium bicarbonate, once with brine, dried with anhydrous sodium sulfate and concentrated in vacuo to give a beige solid. The crude product was recrystallized from 50% ethyl acetate/hexane (220 mL). After 4 days the suspension was filtered, the filter pad was washed with hexanes and then diethyl ether, and dried in vacuo at 55° C. overnight to give 83 (0.20 g, 30%) as a light orange solid. Concentration of the filtrate in vacuo followed by triturating the resulting residue with diethyl ether and filtering off the resulting solid yielded an additional 45 mg of 83 as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124632B2
Source datasetuspto-grants-2012_02
ORD IDord-cc0e14ef450647909e54803c711376a7
Source noteuspto-grants-2012_02