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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 366204Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/366204

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktN-(tert-butoxycarbonyl)glycineHCID 78288—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium BisulfateHCID 516919—
ProduktEthyl 2-((tert-butoxycarbonyl)amino)acetateHCID 35772991,7%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

(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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06127391
Quelldatensatzuspto-grants-2000_10
ORD IDord-65bc166599b3463ba1ae8ea7c1ad5ada
Quellennotizuspto-grants-2000_10