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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496806Generated: October 25, 2026

5-Bromo-2-(methylthio)pyridine → 5-Bromo-2-methanesulfonylpyridine

https://huagongshe.com/reaction/496806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-(methylthio)pyridineHCID 11424251—
ReactantMagnesium 2-(dioxidan-2-ide-1-carbonyl)benzoate--water (1/1/6)HCID 21894687—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-methanesulfonylpyridineHCID 1343342492%

Reaction Steps

5-bromo-2-methylsulfanyl pyridine (3.47 g) was dissolved in a mixed solvent of dichloromethane and methanol with the ratio of 5:1 (v/v) and magnesium monoperoxyphthalate hexahydrate was slowly added dropwise. After completing the reaction for 3 hours at room temperature, magnesium monoperoxyphthalate hexahydrate was filtered out, sodium bicarbonate and salt water was added to dilute, and extracted with dichloromethane to separate an organic layer. The separated organic layer was dried with anhydrous magnesium sulfate and distilled under reduced pressure. As a result, 5-bromo-2-methylsulfonyl pyridine (3.7 g, yield: 92%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946558B2
Source datasetuspto-grants-2005_09
ORD IDord-df17a300a0d6499e9f3c2d8eac9914c3
Source noteuspto-grants-2005_09