A method for reclaiming 3-ethoxyl-4-methoxyl-alpha-[(methylsulfonyl)methyl]-benzylamine
A methylsulfonyl, methoxyphenyl technology, applied in the preparation of carboxylic acid amides, organic chemistry methods, chemical instruments and methods, etc., can solve problems such as unavailability, achieve prevention of solid waste, reduce environmental pollution, The effect of reducing production costs
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Embodiment 1
[0036] (1) Synthesis of Compound II and Compound III
[0037] Based on the weight of Compound I, weigh 100g of Compound I, add 600g of purified water and 9.5g of sodium hydroxide, heat up to 40-80°C, keep warm for 2h, cool down to 10-30°C, and filter to obtain a filter cake and filtrate. Filter cake is compound II wet product, stand-by;
[0038] Add hydrochloric acid to the filtrate to adjust the pH to 2-3, stir at 20-30°C for 1 h, and filter with suction to obtain the wet product of Compound III. The compound III wet product was rinsed with water, the washing liquid was combined into the filtrate, and the compound III wet product was dried to obtain 32.5 g of compound III, with a yield of 83.8%.
[0039] (2) Synthesis of compound IV
[0040] Under stirring, add solid sodium bicarbonate to the filtrate obtained in step (1), adjust the pH of the reaction solution to 7-8, add the wet product of compound II prepared in step (1), heat up to 90-100°C, and keep stirring for 40 hou...
Embodiment 2
[0052] (1) Synthesis of Compound II and Compound III
[0053]Based on the weight of Compound I, weigh 500kg of Compound I, add 3000kg of purified water and 47.5kg of sodium hydroxide, heat up to 40-80°C, keep warm for 2h, cool down to 10-30°C, and filter to obtain a filter cake and filtrate. Filter cake is compound II wet product, stand-by;
[0054] Add hydrochloric acid to the filtrate to adjust the pH to 2-3, stir at 20-30°C for 1 hour, and filter with suction to obtain a wet product of the compound. The wet product of the compound was rinsed with water, the washing liquid was combined into the filtrate, and the wet product of the compound was dried to obtain 150 kg of compound III, with a yield of 77.4%.
[0055] (2) Synthesis of compound IV
[0056] Under stirring, add solid sodium bicarbonate to the filtrate obtained in step (1), adjust the pH of the reaction solution to 7-8, add the wet product of compound II prepared in step (1), heat up to 90-100°C, and keep stirring...
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