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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219671Generated: October 29, 2026

Sodium Thiosulfate → Methyl 2-(methanesulfonyl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/219671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl 2-(Methylthio)pyrimidine-5-carboxylateHCID 11194721—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(methanesulfonyl)pyrimidine-5-carboxylateHCID 5339649190%

Reaction Steps

To a solution of 2-methylsulfanyl-pyrimidine-5-carboxylic acid methyl ester 1 (1 g, 5.43 mmol) in DCM (60 mL) is added MCPBA (2.81 g, 16.29 mmol) portion wise at room temperature. The resulting solution is stirred at room temperature overnight. A solution of Na2S2O3 (1.6 g) in water (60 mL) is added. The mixture is stirred at room temperature for 20 min. The layer is separated, and the water layer is extracted with DCM (2×20 mL). The combined DCM layer is washed with saturated NaHCO3 (3×20 mL), dried (Na2SO4), filtered and concentrated in vacuo to afford 2-methanesulfonyl-pyrimidine-5-carboxylic acid methyl ester as a solid (1.05 g, 90%). MS: 217 (M+H); 1H NMR (300 MHz, CDCl3): δ 3.41 (s, 3H), 4.06 (s, 3H), 9.44 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202863B2
Source datasetuspto-grants-2012_06
ORD IDord-bab0c6a785ff4f04be7cf4774c1a7229
Source noteuspto-grants-2012_06