2-(2-クロロエチル)-2,3-ジヒドロ-4H-1,3-ベンゾオキサジン-4-オン 化学特性,用途語,生産方法
Originator
Reugaril ,Farber ,Italy ,1966
Manufacturing Process
A mixture of 4 liters chloroform and 1,050 cc ethanol was saturated with dry
hydrogen chloride gas at -5°C to +5°C in a vessel having a net volume of 15
liters and provided with a stirring device, reflux cooler, gas feed line,
thermometer and dropping funnel. 455 g acrolein which had been precooled
to 0°C were added dropwise to the solution over a period of 1 to 2 hours
while maintaining the temperature below +5°C and vigorously stirring. 1,070
g salicylamide and 1,080 g glacial acetic acid were added to the resulting
solution of beta-chloropropionaldehyde acetal, thereby forming a suspension
which was heated to 60°C while stirring. A clear solution was formed which
was maintained at 60°C for an additional hour. The solution was allowed to
cool to about 40°C and was then washed with water by passing a strong
stream of water under the surface of the chloroform and continuously
withdrawing the upper phase. When the water had reached a pH of 3-4, the
precipitated reaction product was separated by vacuum filtration. The
chloroform phase of the filtrate was evaporated under a weak vacuum and the
residue was combined with the precipitate first obtained. The combined
products were stirred with 2 liters of a 5% sodium hydroxide solution. The raw
reaction product was then washed with water, dried and recrystallized from
ethanol. The product had the melting point of 146°C to 147°C
(decomposition). The yield was 1,260 g, corresponding to 76% of the
theoretical yield.
Therapeutic Function
Antipyretic, Analgesic
2-(2-クロロエチル)-2,3-ジヒドロ-4H-1,3-ベンゾオキサジン-4-オン 上流と下流の製品情報
原材料
準備製品