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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359485Generated: October 26, 2026

Ethyl chloroformate → Ethyl 1-ethoxycarbonyl-1,2,3,6-tetrahydropyridine-4-carboxylate

https://huagongshe.com/reaction/1359485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 1-methyl-1,2,3,6-tetrahydro-4-pyridinecarboxylateHCID 566021—
SolventBenzeneHCID 241—
ProductEthyl 1-ethoxycarbonyl-1,2,3,6-tetrahydropyridine-4-carboxylateHCID 1254967071.4%

Reaction Steps

In 640 ml of benzene, 108.9 g of ethyl 1-methyl-1,2,3,6-tetrahydropyridine-4-carboxylate and 41.6 g of diisopropylethylamine were dissolved, and subsequently, 279.1 g of ethyl chloroformate was added dropwise thereto over 70 minutes. The reaction mixture was heated under reflux for 30 minutes, followed by cooling the reaction mixture to room temperature. A saturated aqueous solution of sodium hydrogencarbonate was poured thereinto. After the reaction mixture was extracted with ethyl acetate, the extract was washed with saturated brine and was then dried over anhydrous sodium sulfate. The desiccant was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=7:1) to yield 104.4 g of ethyl 1-ethoxycarbonyl-1,2,3,6-tetrahydropyridine-4-carboxylate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06600038B1
Source datasetuspto-grants-2003_07
ORD IDord-33dfa1ee66794f0990d00b7318cda3c2
Source noteuspto-grants-2003_07