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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217256Generated: October 25, 2026

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

https://huagongshe.com/reaction/217256

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% ethyl acetate in hexane to give 0.348 g of the 2-[chloro(difluoro)methyl]-5-[1-(methylthio)ethyl]pyridine (E) in 40% yield GC-MS: mass calcd for C9H10ClF2NS [M]+ 237. Found 237.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193364B2
Source datasetuspto-grants-2012_06
ORD IDord-be10383755d8451592091cca4b6caa26
Source noteuspto-grants-2012_06