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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3-mercaptopropionate | HCID 18050 | — |
| Reactant | Ethyl 4-chloropyridine-3-carboxylate | HCID 14116704 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-Methoxycarbonyl-ethylsulfanyl)-pyridine-3-carboxylic acid ethyl ester | HCID 86720164 | 48.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284286B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-ea005294d66549e0a9b3a95eed2a98eb |
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| Source note | uspto-grants-2016_03 |
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