Реакция #155359
ord-727ba28406384fee9d438a866f21cfd8
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Другое(exothermic reaction)
- 2Другоеto precipitate
- 3Фильтрацияwhich were filtered off
- 4КонцентрированиеThe organic phase was then concentrated down under vacuum in a rotovap
- 5Другоеto afford the product as a residue in the form of a yellow orange oil
Методика
To 5-fluoro-2-nitrotoluene (50.0 g, 0.32 mol) was added sodium carbonate (17.1 g, 0.16 mol) at 60° C. 3,3′-Diamino-N-methyldipropylamine (23.7 g, 0.16 mol) was then carefully added dropwise (exothermic reaction). The resulting mixture was heated at 100° C. for 12 hours. 100 ml toluene were added to the cooled reaction mixture causing the inorganic salts to precipitate, which were filtered off. The organic phase was then concentrated down under vacuum in a rotovap to afford the product as a residue in the form of a yellow orange oil. Yield: 52.5 g (78.4%); 1H-NMR (400 MHz, DMSO-d6): δ [ppm]=1.71 (m, 4H); 2.18 (s, 3H); 2.40 (m, 4H); 2.55 (s, 6H); 3.17 (m, 4H); 6.45 (s, 2H); 6.48 (d, 2H); 7.08 (br., 2×NH); 7.92 (d, 2H).