反应详情

Phenylbutazone (1,2-diphenyl-3,5-pyrazolidinedione; 11.00 g, 0.035 mole) was treated with 11.55 g (0.055 mole) of trifluoroacetic anhydride. The resulting solid suspension was shaken or mechanically stirred until a homogeneous solution was obtained, then it was stirred with a magnetic stirrer at room temperature in a tightly closed flask for one hour. The solution was concentrated in vacuo for one hour and the oily residue obtained was dissolved in 50 ml of acetone and allowed to react with 12.5 g (0.055 mole) of nicotinic anhydride. The initial suspension became homogeneous after 0.25 hours with concomitant formation of a yellow color. After an additional one hour at room temperature, the yellow solution was concentrated in vacuo and the residue was dissolved in 200 ml of dichloromethane. The dichloromethane solution was extracted first with an aqueous sodium bicarbonate solution (12.2 g, 0.145 mole in 150 ml), then with an aqueous sodium hydroxide solution (28 g, 0.07 mole in 56 ml) and subsequently dried over sodium sulfate. The dichloromethane solution was concentrated in vacuo and the residue was crystallized from dichloromethane petroleum ether bp 30°-60° C to give 11.16 g (mp 139°-141° C, 77.5% yield) of the title compound.

1. stirringmechanically stirred until a homogeneous solution
2. customwas obtained
3. stirringit was stirred with a magnetic stirrer at room temperature in a tightly closed flask for one hour
4. concentrationThe solution was concentrated in vacuo for one hour
5. customthe oily residue obtained
6. concentrationthe yellow solution was concentrated in vacuo
7. dissolutionthe residue was dissolved in 200 ml of dichloromethane
8. concentrationThe dichloromethane solution was concentrated in vacuo
9. customthe residue was crystallized from dichloromethane petroleum ether bp 30°-60° C