HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241049Generated: October 29, 2026
Sodium methanesulfinate → HCID 58255826, compound
https://huagongshe.com/reaction/241049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | 5-Bromo-2-chloro-3-(chloromethyl)pyridine | HCID 42544310 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58255826 | HCID 58255826 | 94.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648066B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-593fcaba36af44879fa0e4a56adbc78c |
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| Source note | uspto-grants-2014_02 |
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