(Z)-N-(アミノカルボニル)-2-エチル-2-ブテンアミド

(Z)-N-(アミノカルボニル)-2-エチル-2-ブテンアミド 化学特性,用途語,生産方法

• Originator

  Nostyn,Ames,US,1956

• Manufacturing Process

  54 g of carbromal (2-bromo-2-ethylbutyryl-urea) in 600 cc of isopropanol was stirred and refluxed for 3 hours with 27.8 g of anhydrous silver oxide. The reaction mixture was filtered and the silver residue was extracted with 100 cc of boiling isopropanol. The filtered and dried solids which separated weighed 22.5 g and melted at 189°C to 190.5°C. Concentration of the filtrate yielded an additional 3.3 g of product which melted at 160°C to 170°C. These two crops were separately obtained as white needles by crystallization from alcohol and exhibited slight solubility in water. The first crop gave 21.7 g of 2- ethyl-cis-crotonyl urea with a melting point of 191°C to 193°C, and the second crop gave 0.9 g with a melting point of 191°C to 193°C for a total yield of 42.4 g or 63% of the theoretical.

• Therapeutic Function

  Sedative

(Z)-N-(アミノカルボニル)-2-エチル-2-ブテンアミド 上流と下流の製品情報

(Z)-N-(アミノカルボニル)-2-エチル-2-ブテンアミド 生産企業

Global(7)Suppliers

95-04-5, (Z)-N-(アミノカルボニル)-2-エチル-2-ブテンアミド キーワード