Реакция #1687153
ord-f491c729248d4d28947c17fd6ee5332d
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1workup.ADDITIONare added
- 2ТемператураThe mixture is then heated
- 3Другоеthus obtained
- 4Температураandthe mixture is subsequently refluxed for a further 3 hours
- 5Экстракцияis extracted with methylene chloride
- 6ДругоеAfter drying
- 7Концентрированиеthe organic phase is concentrated
- 8ДругоеThe solid obtained
- 9Другоеis sufficiently pure for the subsequent reaction (NMR)
Методика
49.7 g (0.253 mol) of 2-methyl-3-nitro-6-aminobenzoic acid are dissolved in380 ml of acetone and 43 g (0.51 mol) of sodium hydrogen carbonate are added. The mixture is then heated to boiling until evolution of CO2 is complete. 35.3 g (0.28 mol) of dimethyl sulfate are then added in the course of two hours at the boiling point of acetone to the suspension of the sodium salt of 2-methyl-3-nitro-6-aminobenzoic acid thus obtained, andthe mixture is subsequently refluxed for a further 3 hours and then allowedto cool. After pouring the reaction mixture into 1.8 l of water, it is extracted with methylene chloride. After drying, the organic phase is concentrated. The solid obtained is sufficiently pure for the subsequent reaction (NMR). Yield: 50 g (0.238 mol)=94% of theory, m.p.: 92°-94° C.