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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991065Generated: 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/991065

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), 10N 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 numberUS06462073B2
Source datasetuspto-grants-2002_10
ORD IDord-18ee37c734104b71bc982a9f21d357b8
Source noteuspto-grants-2002_10