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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237426Generated: October 31, 2026

Ethyl chloroformate → [Ethoxycarbonyl-(2-thiophen-2-yl-ethyl)-amino]acetic acid ethyl ester

https://huagongshe.com/reaction/2237426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantEthyl oxoacetateHCID 70211—
ReactantThiopheneethanamineHCID 116521—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product[Ethoxycarbonyl-(2-thiophen-2-yl-ethyl)-amino]acetic acid ethyl esterHCID 66934051—

Reaction Steps

2-Thiophen-2-yl-ethylamine (21 g, 165 mmol) was stirred in 1 liter of DCM. Ethyl glyoxylate (165 mmol, 50% in toluene) was added followed by 50 uL HOAc. The reaction was stirred for 10 minutes after which time NaBH(OAc)3 (214 mmol, 45 g) was added slowly. After 15 minutes HOAc was added (214 mmol) and the reaction was stirred for 20 minutes. The reaction was concentrated and the crude material was dissolved in 500 mL each of THF and water. NaHCO3 (42 g, 500 mmol) was added followed by ethyl chloroformate (21 mL, 214 mmol). Saturated NaHCO3 was added slowly to the reaction until the gas evolution was minimal. After stirring overnight, the reaction was diluted with EtOAc (400 mL). The product was extracted 2× into EtOAc, dried over MgSO4, and concentrated to give the subtitle product as a dark oil that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718647B2
Source datasetuspto-grants-2010_05
ORD IDord-59d7e72124d04a2f85fc5880f87c0a95
Source noteuspto-grants-2010_05