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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531062Generated: November 1, 2026

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

https://huagongshe.com/reaction/1531062

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 numberUS06197791B1
Source datasetuspto-grants-2001_03
ORD IDord-646a42c3edf64e6da8f42f7f599f08a2
Source noteuspto-grants-2001_03