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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302235Generated: October 31, 2026

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

https://huagongshe.com/reaction/2302235

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 numberUS06432951B1
Source datasetuspto-grants-2002_08
ORD IDord-1d23eabcdc6f47beb7b8bb9b66b7aa8b
Source noteuspto-grants-2002_08