Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184663Generated: November 1, 2026

Sodium methanethiolate → 5-[1-(Methylthio)ethyl]-2-(trichloromethyl)pyridine

https://huagongshe.com/reaction/1184663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant5-(1-Bromoethyl)-2-(trichloromethyl)pyridineHCID 59218638—
SolventEthanolHCID 702—
Product5-[1-(Methylthio)ethyl]-2-(trichloromethyl)pyridineHCID 59218620—

Reaction Steps

A solution of 5-(1-bromoethyl)-2-(trichloromethyl)pyridine (A) (0.95 g, 3.14 mmol) in ethanol (15 mL) was treated with sodium thiomethoxide (0.44 g, 6.29 mmol) portionwise at 0° C. The mixture was stirred at room temperature overnight. The solvent ethanol was then removed under a reduced pressure and the residue was re-taken into CH2Cl2 and brine. The two phases were separated and the organic layer was dried over anhydrous Na2SO4, filtered, concentrated. The residue was purified on silica gel using 5% EtOAc in hexane to give 0.57 g of the partially pure 5-[1-(methylthio)ethyl]-2-(trichloromethyl)pyridine (B) in 67% crude yield. GC-MS: mass calcd for C9H10Cl3NS [M]+ 269. Found 269.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669278B2
Source datasetuspto-grants-2014_03
ORD IDord-306fdf6bfb524aa4b5e4a70c52a9c2fc
Source noteuspto-grants-2014_03