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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270347Generated: October 30, 2026

3-(Chloromethyl)pyridine hydrochloride → 2-(4-Methoxy-benzensulfonyl)-2-methyl-3-pyridin-3-yl-propionic acid ethyl ester

https://huagongshe.com/reaction/2270347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
Reactant2-(4-Methoxy-benzenesulfonyl)propionic acid ethyl esterHCID 20660503—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product2-(4-Methoxy-benzensulfonyl)-2-methyl-3-pyridin-3-yl-propionic acid ethyl esterHCID 11046694—

Reaction Steps

To a stirred solution of 2-(4-methoxy-benzenesulfonyl)propionic acid ethyl ester (2.7 gm, 10 mmol), 3-picolyl chloride hydrochloride (3.2 g, 20 mmol). and triethyl benzylammonium chloride (1 g) in methylene chloride (400 ml), 10 N NaOH (30 ml) was added. The reaction was continued at room temp for 48 hours. At the end, the organic layer was separated and washed well with water. The organic layer was dried, filtered and concentrated. The crude product obtained was purified by silica-gel column chromatography. The column was eluted with 50% ethyl acetate: hexane. 2-(4-Methoxy-benzensulfonyl)-2-methyl-3-pyridin-3-yl-propionic acid ethyl ester was isolated as brown oil. Yield 3.0 g, 82%; Brown oil; MS: 364 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331563B1
Source datasetuspto-grants-2001_12
ORD IDord-62a297592bfb46609f00de6a7d5e0d53
Source noteuspto-grants-2001_12