Reaktion #430928
ord-2969ee246e8847f390c9589c6bc88f54
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturThe mixture is then heated
- 2Sonstigethus obtained
- 3Temperaturthe mixture is subsequently refluxed for a further three hours
- 4Temperaturto cool
- 5Extraktionis extracted with methylene chloride
- 6SonstigeAfter drying
- 7Einengenthe organic phase is concentrated
- 8SonstigeThe solid obtained
- 9Sonstigeis sufficiently pure for the subsequent reaction (NMR)
Vorschrift
49.7 g (0.253 mol) of 2-methyl-3-nitro-6-aminobenzoic acid are dissolved in 380 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 dropwise 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, and the mixture is subsequently refluxed for a further three hours and then allowed to 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.