HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990703Generated: October 27, 2026
Triethylamine → Ethyl N-(ethyl carboxymethyl)oxamate
https://huagongshe.com/reaction/990703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | 2-(Ethylamino)acetic acid hydrochloride | HCID 19011402 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Ethyl N-(ethyl carboxymethyl)oxamate | HCID 18621232 | — |
Reaction Steps
To a suspension of ethyl glycine·HCl 2 (38.4 g, 275 mmol) in 1,2-dichloroethane (360 mL) was added triethylamine (77.0 mL, 550 mmol) at room temperature. After stirring for 30 minutes the heterogenous mixture was cooled to 0° C. and ethyl oxalyl chloride 1 (30.3 mL, 275 mol) was added dropwise over the course of 1 h. Upon completion of the addition, the cooling bath was removed and the reaction was stirred at room temperature overnight. The reaction was diluted with water (250 mL) and the layers separated. The aqueous layer was backwashed with 2 portions of dichloromethane (250 mL). The combined organic layers were washed with water (250 mL), followed by brine (250 mL), dried over MgSO4 and concentrated to give an oil 3 that was taken directly onto the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06462050B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-3261838be3f34ce08df745d2ec1cf0cd |
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| Source note | uspto-grants-2002_10 |
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