Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302237Generated: October 31, 2026

Dimethylformamide → 5-(1-Benzoyloxymethyl)-3-chloro-2-methylthiopyridine

https://huagongshe.com/reaction/2302237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloro-5-(1-hydroxyethyl)-2-methylthiopyridineHCID 18435800—
SolventWaterHCID 962—
Product5-(1-Benzoyloxymethyl)-3-chloro-2-methylthiopyridineHCID 1846053979%

Reaction Steps

3-Chloro-5-(1-hydroxyethyl)-2-methylthiopyridine (21.9 g, 0.108 mol) was dissolved with stirring in anhydrous DMF (250 mL) and 60% sodium hydride (5 g, 0.125 mol) added in portions. The mixture was stirred at room temperature for 30 minutes and benzyl bromide (17.6 g, 0.103 mol) added dropwise. The mixture was then stirred at room temperature for four hours, diluted with water (400 mL) and extracted three times with ethyl acetate (100 mL). The combined organic extracts were washed twice with water (200 mL) and saturated sodium chloride solution (100 mL), dried over anhydrous sodium sulphate, and evaporated to dryness. Purification of the residue by chromatography over silica (0-5% ethyl acetate:hexane) gave the desired product (25.0 g, 79%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432951B1
Source datasetuspto-grants-2002_08
ORD IDord-b3fd9e405cec4ec08f881ce16dec9ad2
Source noteuspto-grants-2002_08