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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925267Generated: October 26, 2026

Methyl 3-mercaptopropionate → 4-(2-Methoxycarbonyl-ethylsulfanyl)-pyridine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/925267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-mercaptopropionateHCID 18050—
ReactantEthyl 4-chloropyridine-3-carboxylateHCID 14116704—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Methoxycarbonyl-ethylsulfanyl)-pyridine-3-carboxylic acid ethyl esterHCID 8672016448.3%

Reaction Steps

To a stirred solution of 4-chloro-pyridine-3-carboxylic acid ethyl ester (4.30 g, 23.2 mmol) in dry tetrahydrofuran (45 ml) is added potassium tert-butoxide (3.12 g, 27.9 mmol) portion wise at 0° C., followed by the addition of methyl 3-mercaptopropanoate (3.35 g, 27.9 mmol). The reaction mixture is stirred at RT for 2 h. After completion of the reaction, the solvent is distilled off and the residue is diluted with water (30 ml). The aqueous layer is extracted with EtOAc (3×40 ml). The combined organic layers are washed with water (40 ml), brine (40 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 30% EtOAc/hexane) to get 4-(2-methoxycarbonyl-ethylsulfanyl)-pyridine-3-carboxylic acid ethyl ester (3.0 g, 11.2 mmol, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284286B2
Source datasetuspto-grants-2016_03
ORD IDord-ea005294d66549e0a9b3a95eed2a98eb
Source noteuspto-grants-2016_03