Crystal form of nicosulfuron and preparation method thereof
A nicosulfuron-methyl and crystal form technology is applied to the crystal form of nicosulfuron-methyl and the field of preparation thereof, which can solve the problems of not overcoming nicosulfuron-methyl and the like, achieve accurate calibration of product content, and ensure stability and accuracy. Effect
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[0031] (1) Take a clean 1000mL four-neck flask, put 800mL of acetonitrile into it, heat it in a water bath to 55°C while stirring (the boiling point of acetonitrile is 63°C), take 100g of high-content nicosulfuron original drug (all impurities are relatively low, content greater than or equal to 95%), put it into it, stir for 20min, use sand core funnel to suction filter while it is hot, and discard the filter residue;
[0032] (2) The filtrate is quickly placed in another clean 1000mL four-neck flask, and cooled naturally while stirring (if the room temperature is too low, use a water bath to cool naturally at 50°C) to room temperature, and pump it out with another clean sand core funnel. Filter, obtain the nicosulfuron pure product of 30g;
[0033] (3) Place the pure product in a constant temperature drying oven, and dry it for 5 hours at 60°C.
[0034] (4) Take another clean 1000mL four-neck flask, one side is connected with an oil-water separator, and the upper part is co...
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