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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381961Generated: October 31, 2026

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

https://huagongshe.com/reaction/2381961

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 g, 5.43 mmol) in DCM (60 mL) is added MCPBA (2.81 g, 16.29 mmol) portion wise at rt. The resulting solution is stirred at rt overnight. A solution of Na2S2O3 (1.6 g) in water (60 mL) is added. The mixture is stirred at rt for 20 min. The organic layer and aqueous layer are separated, and the aqueous layer is extracted with DCM (2×20 mL). The combined organic layer is washed with saturated aqueous NaHCO3 (3×20 mL), dried (Na2SO4), filtered and concentrated in vacuo to afford 2-methanesulfonyl-pyrimidine-5-carboxylic acid methyl ester (1.05 g, 90%) as a solid. 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 numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-c2fbc95ae24245038e7ce9692163b307
Source noteuspto-grants-2012_09