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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381232Generated: October 31, 2026

Sodium methanethiolate → 5-Acetyl-3-chloro-2-methylthiopyridine

https://huagongshe.com/reaction/381232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant1-(5,6-Dichloropyridin-3-yl)ethan-1-oneHCID 10198006—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Solventtert-ButanolHCID 6386—
Product5-Acetyl-3-chloro-2-methylthiopyridineHCID 1843580294%

Reaction Steps

5-Acetyl-2,3-dichloropyridine (24.5 g, 0.129 mol) was slurried in t-butanol (200 mL) and sodium methanethiolate (10 g, 0.143 mol) was added. The mixture was heated under reflux conditions for two hours, cooled to room temperature, and diluted with water (200 mL) and ether (150 mL). This was separated and the aqueous phase extracted with ether (50 mL). The combined organic extracts were washed with water (100 mL) and saturated sodium chloride solution (100 mL), dried over anhydrous sodium sulphate, and evaporated to dryness to give the desired product (24.1 g, 94%) as a pale, low melting solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306839B1
Source datasetuspto-grants-2001_10
ORD IDord-22e50e9e43b14f3b9775de1aa16d5e0d
Source noteuspto-grants-2001_10