2-METHYL-N-PHENYL-PROPANAMIDE

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: First, 26.2 g of aniline, 100 mL of tetrahydrofuran (THF), and 56.9 g of triethylamine (Et3N) were put in a 500 mL three-neck flask, and mixed. Then, under cooling in ice, a mixed solution of 30 g of isobutyryl chloride and 100 mL of THF was dripped through a 50 mL dropping funnel to the above mixed solution, and then the temperature was increased to room temperature and the solution was stirred for 19 hours to be reacted. After the reaction, this mixture was subjected to suction filtration to give a filtrate. The resulting filtrate was washed with water, and then saturated saline, and anhydrate magnesium sulfate was added for drying. After the drying, the mixture was subjected to gravity filtration, and the filtrate was concentrated, so that N-phenylisobutyramide was prepared (a white solid, yield: 91%). The synthetic scheme of Step 1 is shown by (a-10). mixed Then, under cooling in ice to be reacted After the reaction this mixture was subjected to suction filtration to give a filtrate The resulting filtrate was washed with water saturated saline, and anhydrate magnesium sulfate was added for drying After the drying, the mixture was subjected to gravity filtration the filtrate was concentrated, so that N-phenylisobutyramide was prepared (a white solid, yield: 91%)