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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366204Generated: October 26, 2026

Ethanol → Ethyl 2-((tert-butoxycarbonyl)amino)acetate

https://huagongshe.com/reaction/366204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventSodium BisulfateHCID 516919—
ProductEthyl 2-((tert-butoxycarbonyl)amino)acetateHCID 35772991.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

(tert-Butoxycarbonylamino)acetic acid (4.00 g, 22.8 mmol) was dissolved in dichloromethane (8 ml). Ethanol (1.60 ml, 27.40 mmol) and 4-dimethylaminopyridine (0.31 g, 25.1 mmol) were added. The solution was cooled to 0° C. N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (4.81 g, 25.11 mmol) was added. The solution was stirred for 16 h, while warming up to room temperature. It was diluted with ethyl acetate (150 ml) and 10% aqueous sodium hydrogen sulfate solution (100 ml). The phases were separated. The aqueous phase was extracted with ethyl acetate (4×50 ml). The combined organic layers were washed with saturated sodium hydrogen carbonate solution (150 ml) and dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (100 g), using ethyl acetate/heptane (1:4) as eluent, to give 4.25 g of ethyl 2-(tert-butoxycarbonylamino)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127391
Source datasetuspto-grants-2000_10
ORD IDord-65bc166599b3463ba1ae8ea7c1ad5ada
Source noteuspto-grants-2000_10