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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595152Generated: October 26, 2026

Sodium Thiosulfate → 2-Chloro-4-(methanesulfonyl)pyrimidine

https://huagongshe.com/reaction/595152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-4-(methylthio)pyrimidineHCID 16427148—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-(methanesulfonyl)pyrimidineHCID 19771379—

Reaction Steps

mCPBA (3.92 g, 17.5 mmol) was added to a stirred mixture of 2-chloro-4-(methylsulfanyl)pyrimidine (1.5 g, 7.0 mmol) in dichloromethane (35.0 mL) at 0° C. The reaction mixture was warmed to room temperature, stirred for 1.5 h and then diluted with aqueous sodium thiosulfate. The solution was stirred for 10 min then saturated sodium bicarbonate was added and the mixture was extracted with dichloromethane. The combined organics were washed with brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (0 to 100% EtOAc/hexanes) to afford 2-chloro-4-(methylsulfonyl)pyrimidine as a white solid. MS ESI calcd. for C5H6C1N2O2S [M+H]+ 193. found 193.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-6e2e90bdaf0e4e19847728ccaace99be
Source noteuspto-grants-2016_01