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HRID 25916Erstellt: 24. Oktober 2026

Ethyl Bromide → Carbamic acid, N-ethyl-, 2-((2-cyanoethyl)phenylamino)ethyl ester

https://huagongshe.com/de/reaction/25916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
EduktSulfolaneHCID 31347—
EduktPropanenitrile, 3-[(2-hydroxyethyl)phenylamino]-HCID 113349—
EduktPotassium cyanateHCID 11378442—
LösungsmittelWaterHCID 962—
ProduktCarbamic acid, N-ethyl-, 2-((2-cyanoethyl)phenylamino)ethyl esterHCID 113132—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Into a 500 ml. three-necked round-bottomed flask equipped with thermometer, stirrer, reflux condenser, and dropping funnel are placed 40 g. (0.493 mole) of potassium cyanate and 250 ml. of sulfolane (tetrahydrothiophene-1,1-dioxide). This mixture is heated with stirring to 90° C. by means of an oil bath. Bromoethane (95 g., 0.8 mole) is then added dropwise to the mixture over a 1.5 hour period. The temperature of the reaction mixture drops to 75° C. during the addition of bromoethane. A solution of 50 g. (0.228 mole, 86.5%) N-(2-cyanoethyl)-N-(2-hydroxyethyl) aniline in 50 ml. of sulfolane is added, and heating of the resulting mixture is continued at 90° C. for three hours. The reaction mixture is cooled to room temperature and then poured into 2 liters of cold water. The mixture is agitated for 0.5 hour, and the two resulting layers separated. TLC of the organic layer in 4:1 benzene:acetone shows only a trace of starting material. The infrared spectrum of the product of the above formula shows absorptions at 3370, 2250, 1915, 1680, and 596 cm-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04147716
Quelldatensatzuspto-grants-1979_04
ORD IDord-a0a3b9ed9b4f48ae977754f28469faf6
Quellennotizuspto-grants-1979_04