HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106648Generated: October 31, 2026
Ethyl chloroformate → Ethyl 4-(hydroxymethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/2106648
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (Piperidin-4-yl)methanol--hydrogen chloride (1/1) | HCID 24191744 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 4-(hydroxymethyl)piperidine-1-carboxylate | HCID 19773576 | 100% |
Reaction Steps
168.3 g (1.22 mol) of potassium carbonate are added to a solution of 61.6 g (406 mmol) of 4-piperidinemethanol hydrochloride in a mixture of 406 ml of chloroform and 406 ml of water, followed by 42.55 ml (440 mmol) of ethyl chloroformate dissolved in 160 ml of chloroform. The mixture is stirred for 3 h at 20° C., the organic phase is separated off, the aqueous phase is extracted with dichloromethane, the organic phases are combined to form a single phase, washed with water and dried over magnesium sulphate, and the solvents are evaporated off under reduced pressure. 76 g of an oil is obtained, this being used without further treatment in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04931449 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-6f6469db1ac847fb9c1db74b98387df3 |
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| Source note | uspto-grants-1990_06 |
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