참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Bromide | HCID 6332 | — |
| 반응물 | Sulfolane | HCID 31347 | — |
| 반응물 | Propanenitrile, 3-[(2-hydroxyethyl)phenylamino]- | HCID 113349 | — |
| 반응물 | Potassium cyanate | HCID 11378442 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Carbamic acid, N-ethyl-, 2-((2-cyanoethyl)phenylamino)ethyl ester | HCID 113132 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04147716 |
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| 출처 데이터셋 | uspto-grants-1979_04 |
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| ORD ID | ord-a0a3b9ed9b4f48ae977754f28469faf6 |
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| 출처 메모 | uspto-grants-1979_04 |
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