Preparation method of 6-nitrosaccharin
A technology of nitrosaccharin and nitrobenzoic acid, applied in the field of preparation of 6-nitrosaccharin, can solve the problems of difficulty in industrialization, serious environmental pollution, difficult control, etc., and achieves low price, no environmental pollution and low production cost Effect
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Embodiment 1
[0019] The preparation method of 6-nitrosaccharin of this embodiment has the following steps:
[0020] ①Preparation of methyl 2-amino-4-nitrobenzoate: Add 40g of 2-amino-4-nitrobenzoic acid and 300ml of methanol (237g) into a 500ml four-necked flask as the reactants, and add 54g of Thionyl chloride is used as an acid catalyst to generate a reaction of 2-amino-4-nitrobenzoic acid methyl ester. The reaction slowly exotherms to boiling, and the reaction is heated and refluxed for 10 hours after dropping. After the completion of the reaction, vacuum was applied under reduced pressure to evaporate the methanol, and the methanol was recovered. The remaining concentrate was dissolved by adding 300 ml of ethyl acetate, and the resulting mixture was washed with a saturated aqueous sodium bicarbonate solution until neutral. Heat the entire system to evaporate the water, continue heating to evaporate the ethyl acetate and concentrate the organic phase to make the product precipitate. After ...
Embodiment 2
[0025] The preparation methods of Example 2 to Example 3 are basically the same as that of Example 1, except that the acid catalyst used in step ① is different. The acid catalyst used in Example 2 is concentrated sulfuric acid (98wt%). Example 3 The acid catalyst used is gaseous hydrogen chloride. The method for adding concentrated sulfuric acid in Example 2 is dropwise addition, and the method for adding gaseous hydrogen chloride in Example 3 is to pass the gaseous hydrogen chloride into the reaction system. See Table 1 for details.
[0026] Table 1
[0027] Acid catalyst
Embodiment 4 to Embodiment 8
[0029] The preparation methods of Example 4 to Example 8 are basically the same as that of Example 1, except that the acidic medium and diazotization temperature used in step ② are different. See Table 2 for details.
[0030] Table 2
[0031] Acid medium
[0032] It can be seen from Table 2 that the yield at the reaction temperature of 10°C to 15°C is higher than other temperatures. On the other hand, the acidic medium is different, and the reaction effect is also different. Using hydrochloric acid as the reaction medium is better than other reaction media.
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