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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25916생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물SulfolaneHCID 31347—
반응물Propanenitrile, 3-[(2-hydroxyethyl)phenylamino]-HCID 113349—
반응물Potassium cyanateHCID 11378442—
용매WaterHCID 962—
생성물Carbamic acid, N-ethyl-, 2-((2-cyanoethyl)phenylamino)ethyl esterHCID 113132—

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04147716
출처 데이터셋uspto-grants-1979_04
ORD IDord-a0a3b9ed9b4f48ae977754f28469faf6
출처 메모uspto-grants-1979_04