HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487335Generated: October 29, 2026
Triethylamine → N-butyloxycarbonyl-amino malonic acid diethyl ester
https://huagongshe.com/reaction/487335
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butyl chloroformate | HCID 61140 | — |
| Reactant | Ethyl aminomalonate hydrochloride | HCID 20464734 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-butyloxycarbonyl-amino malonic acid diethyl ester | HCID 21805915 | 96.4% |
Reaction Steps
To an ice-cold suspension of 15 g (70.87 mmol) of amino malonic acid ethyl ester hydrochloride in 180 ml of methylene chloride, 10.8 g (75 mmol) of chloroformic acid butyl ester and then 14.7 g (145 mmol) of triethylamine were added within several minutes. In this case the temperature was constantly maintained under 20° C. After the addition was completed, the reaction was stirred for another 75 minutes at room temperature. The reaction solution was diluted with 80 ml of CH2Cl2, washed with two portions of water, and dried on Na2SO4. After concentration by evaporation on a rotary evaporator, 18.8 g (96 percent) of pure title product was obtained. Other data concerning the product was:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05294710 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-b322bd32afe2486a89381f5cb94636c0 |
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| Source note | uspto-grants-1994_03 |
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