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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241049Generated: October 29, 2026

Sodium methanesulfinate → HCID 58255826, compound

https://huagongshe.com/reaction/241049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanesulfinateHCID 2733271—
Reactant5-Bromo-2-chloro-3-(chloromethyl)pyridineHCID 42544310—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58255826HCID 5825582694.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 5-bromo-2-chloro-3-(chloromethyl)pyridine (124 mg, 0.52 mmol) and sodium methanesulfinate (52 mg, 0.52 mmol) in dioxane (1.4 mL) and water (1.4 mL) was heated to 110° C. in a microwave reactor for 15 min. After cooling to rt, water was added to the reaction mixture which was subsequently extracted twice with ethyl acetate. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo to provide 5-bromo-2-chloro-3-(methylsulfonylmethyl)pyridine (140 mg, 0.49 mmol, 94% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 8.63 (d, 1H), 8.21 (d, 1H), 4.70 (s, 2H), 3.10 (s, 3H); MS (EI) for C7H7BrClNO2S: 284, 286, 288 (Br+Cl isotopes, MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648066B2
Source datasetuspto-grants-2014_02
ORD IDord-593fcaba36af44879fa0e4a56adbc78c
Source noteuspto-grants-2014_02