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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891313Generated: October 29, 2026

Sodium methanethiolate → 2-[Chloro(difluoro)methyl]-5-[1-(methylthio)ethyl]pyridine

https://huagongshe.com/reaction/1891313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
ReactantPyridine, 2-(chlorodifluoromethyl)-5-(1-chloroethyl)-HCID 59218619—
SolventEthanolHCID 702—
Product2-[Chloro(difluoro)methyl]-5-[1-(methylthio)ethyl]pyridineHCID 5921859540.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-[chloro(difluoro)methyl]-5-(1-chloroethyl)pyridine (D) (0.81 g, 3.6 mmol) in ethanol (10 mL) was added sodium thiomethoxide (0.52 g, 7.4 mmol) under stirring in one portion at 0° C. After 10 min, the mixture was allowed to warm to room temperature and stirred overnight. The solvent ethanol was then removed under reduced pressure and the residue was re-taken into ether/CH2Cl2 and brine. The two phases were separated and the organic layer was extracted with CH2Cl2 one more time. The combined organic layer was dried over anhydrous Na2SO4, filtered, concentrated, purified on silica gel using 5 percent ethyl acetate in hexane to give 0.348 g of the 2-[chloro(difluoro)methyl]-5-[1-(methylthio)ethyl]pyridine (E) in 40 percent yield GC-MS: mass calcd for C9H10ClF2NS [M]+ 237. Found 237.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507532B2
Source datasetuspto-grants-2013_08
ORD IDord-53bf3a579ccd4ca8919355e0d87523ae
Source noteuspto-grants-2013_08