تفاعل #1256716
ord-f85afddd930841fabddb2b6d70317912
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1workup.STIRRINGThe reaction mixture was next stirred at 85° C. under N2 for 5 h
- 2أخرىThe solvent was then removed under reduced pressure
- 3غسيلThe resulting solid was washed with benzene (20 mL)
- 4workup.DISSOLUTIONdissolved in water
- 5ترشيحfiltered
- 6أخرىto give a dark-yellow aqueous solution
- 7ترشيحthe resulting yellow precipitate was collected by filtration
- 8أخرىto give an orange solid
- 9أخرىThe crude product was purified by flash chromatography on silica gel eluting with 1:1 hexane
الإجراء التجريبي
To an ice-cooled suspension of NaH (0.12 g, 5.0 mmol) in anhydrous 1,2-dimethoxyethane (8 mL) was added dropwise via syringe a solution of malononitrile (0.165 g, 2.50 mmol) in anhydrous 1,2-dimethoxyethane (2 mL) under N2. The mixture was stirred for 1 h at room temperature under N2. Next, 11 (0.674 g, 2.00 mmol) and tetrakis(triphenyphophine)palladium(0) (0.232 g, 0.200 mmol) were added to the resulting pink suspension under an N2 flow. The reaction mixture was next stirred at 85° C. under N2 for 5 h. The solvent was then removed under reduced pressure. The resulting solid was washed with benzene (20 mL), dissolved in water, and filtered to give a dark-yellow aqueous solution. This solution was neutralized with 5% HCl to pH=7, and the resulting yellow precipitate was collected by filtration to give an orange solid. The crude product was purified by flash chromatography on silica gel eluting with 1:1 hexane: ethyl acetate, to give 0.525 g (95.5%) of the title compound as red solid: mp 58-60° C.; 1H NMR (400 MHz, CDCl3): δ 8.412 (s, 2H), 7.286 (s, 2H), 5.100 (s, 1H), 1.946 (s, 6H), 1.895 (s, 6H); 13C NMR (100 MHz, CDCl3): δ 149.066, 146.564, 139.513, 137.283, 130.441, 126.692, 125.518, 112.024,28.059, 19.988, 16.704; Anal. Calcd. for C18H17N3·H2O: C, 73.69; H, 6.53; N, 14.32. Found; C, 73.36; H, 6.35; N, 14.07.