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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659044Generated: October 30, 2026

Triethylamine → ethyl 3-[ethoxycarbonyl-(2-ethoxy-2-oxoethyl)amino]propanoate

https://huagongshe.com/reaction/659044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 12887440HCID 12887440—
SolventDichloromethaneHCID 6344—
Productethyl 3-[ethoxycarbonyl-(2-ethoxy-2-oxoethyl)amino]propanoateHCID 438161765.1%

Reaction Steps

Crude intermediate (c) (418 mmol) was dissolved in CH2Cl2 (275 mL) and triethylamine (58.3 mL, 418 mmol) was added followed by ethyl chloroformate (d) (39.8 mL, 418 mmol). The reaction was stirred at ambient temperature for about 24 h. After the reaction was complete, the volatile components were removed under vacuum. The crude product was then distilled under vacuum (about 5 mm Hg) and dissolved in EtOAc which was washed with aqueous saturated KHSO4×3, with brine×1 and dried over Na2SO4. Following filtration, the volatile components were removed under vacuum to afford intermediate (e) as a clear oil (74.8 g, 272 mmol) in 65% yield over two steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080556B2
Source datasetuspto-grants-2011_12
ORD IDord-458e5b3470394c35befca18d4ab875ad
Source noteuspto-grants-2011_12