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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 1-methyl-1,2,3,6-tetrahydro-4-pyridinecarboxylate | HCID 566021 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 1-ethoxycarbonyl-1,2,3,6-tetrahydropyridine-4-carboxylate | HCID 12549670 | 71.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06600038B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-33dfa1ee66794f0990d00b7318cda3c2 |
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| Source note | uspto-grants-2003_07 |
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