Process for producing O, S-dimethyl-N-acetylphosphoramidothioate
A technology of acetyl thiophosphoramidide and dimethyl thiophosphoramidide acetyl, applied in the improved O field, can solve problems such as high production cost, non-biodegradation, harsh operating conditions, etc., achieves improved production operating environment, reduced Production cost, effect of simplifying process facilities
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Embodiment 1
[0010] In a 1000ml three-neck flask equipped with stirring, ice-salt bath, thermometer, and dropping funnel, add 216.9 grams of O, S-dimethylphosphorothioate with a content of 65%, and slowly add 155 grams of ethyl alcohol from the dropping funnel. For acid anhydride, cool down to 10°C with an ice-salt bath, slowly add 2 grams of 98% sulfuric acid dropwise, and control the temperature of dropping sulfuric acid at 20-25°C. Then, change the water bath to heat, react at 55-60°C for 1 hour, cool down to 20°C, add about 230ml of 25% sodium carbonate solution to pH=7-9 through the dropping funnel, and control the neutralization temperature at 20-30°C. Then, stand and separate layers, use 1,2-dichloroethane or trichloromethane to extract the lower oil phase and the upper water phase respectively, combine the extracts, and vacuum precipitation, crystallization or recrystallization, and drying, can be Obtained 197.8 grams of O, S-dimethyl-N-acetylphosphorothioate product. The O, S-dim...
Embodiment 2
[0013] In a 1000ml three-necked flask equipped with stirring, ice-salt bath, thermometer, and dropping funnel, add 100 grams of O, S-dimethylphosphorothioate with a content of 65%, and slowly add 52 grams of B For acid anhydride, cool down to 10°C with an ice-salt bath, slowly add 1 gram of 98% sulfuric acid dropwise, and control the temperature of the dropwise addition of sulfuric acid at 20-25°C. Then, change the water bath to heat, react at 55-60°C for 1 hour, cool down to 20°C, add about 500ml of 8% sodium bicarbonate solution from the dropping funnel to pH = 7-9, and control the neutralization temperature at 20-30°C . Then, stand and separate layers, use 1,2-dichloroethane or trichloromethane to extract the lower oil phase and the upper water phase respectively, combine the extracts, and vacuum precipitation, crystallization or recrystallization, and drying, can be Obtained 84 grams of O, S-dimethyl-N-acetylphosphorothioate product. The O,S-dimethyl-N-acetylthiophosphor...
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