비미놀

비미놀 화학적 특성, 용도, 생산

• Originator

  Dividol ,Zambon ,Italy ,1974

• Manufacturing Process

  10 g (0.0278 mol) of 1-(o-chloro)-benzyl-2-di-sec-butylaminoacetyl-pyrrole and 300 ml of anhydrous diethyl ether are placed in a 500 ml four-necked flask with a mercury-sealed stirrer, a thermometer, a dropping funnel and a reflux condenser topped with a tube containing anhydrous calcium chloride. The solution is stirred and a mixture of 1g (0.0264 mol) of lithium aluminum hydride in 20 ml of diethyl ether is added slowly through the dropping funnel at such a rate that the solvent refluxes gently without external heating. When the addition is complete and the initial reaction subsides, the mixture is stirred and heated at gentle reflux for two hours.
  The mixture is cooled and the excess of lithium aluminum hydride is decomposed with cracked ice. The water layer is separated and washed with diethyl ether. The combined ether extracts are dried over anhydrous magnesium sulfate and the solvent is removed by distillation under reduced pressure. Yield, 8.8 g; boiling point, 160°C to 165°C/0.1 mm Hg.

• Therapeutic Function

  Analgesic

비미놀 준비 용품 및 원자재

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