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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 495800Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/495800

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
PatentnummerUS06939880B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-90582ce327074410882fb9b84df6a20b
Quellennotizuspto-grants-2005_09