Preparation method of 2-bromine-5-fluorine trifluorotoluene
A technology of fluorotrifluorotoluene and m-fluorotrifluorotoluene, which is applied in the field of organic synthesis, can solve the problems of difficulty in obtaining a brominating reagent, high processing costs, unfriendly environment, etc., and achieves low price, few reaction steps, and easy raw materials. effect of purchase
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Embodiment 1
[0023] Add 6.00kg of 70% sulfuric acid into a 10L glass reactor, pass through frozen brine, control the temperature below 30°C, add 0.66kg of m-fluorobenzotrifluoride under stirring, heat the mixture to keep the temperature at 45-50°C, divide Add 0.80kg powdered potassium bromate in 10 batches for about 4 hours. After the addition, continue to keep warm and stir for 2 hours. Take samples for analysis until the reaction is complete, quench, extract with 3L dichloromethane, wash with sodium sulfite, remove the solvent after alkali washing, and rectify The 158-162°C / 760mmHg fraction was collected to obtain a product with a weight of 0.92kg, a purity of 99.2%, and a yield of 93.9%.
Embodiment 2
[0025] Add 6.00kg of 70% sulfuric acid into a 10L glass reactor, pass through frozen brine, control the temperature below 30°C, add 0.66kg of m-fluorobenzotrifluoride under stirring, heat the mixture to keep the temperature at 45-50°C, divide Add 1.00kg powdered potassium bromate in 10 batches for about 4 hours. After the addition, continue to keep warm and stir for 2 hours. Take samples for analysis until the reaction is complete, quench, extract with 3L dichloromethane, wash with sodium sulfite, remove the solvent after alkali washing, and rectify The 158-162°C / 760mmHg fraction was collected to obtain a product with a weight of 0.91kg, a purity of 99.0%, and a yield of 92.7%.
Embodiment 3
[0027] Add 6.00kg of 70% sulfuric acid into a 10L glass reactor, pass through frozen brine (water bath, the same below), control the temperature below 30°C, add 0.66kg of m-fluorobenzotrifluoride under stirring, and heat the mixture to keep the temperature at 30~35℃, add 0.80kg powdered potassium bromate in 10 batches, about 4 hours, continue to keep warm and stir for 2 hours after adding, take samples and analyze until the reaction is completed, quench, extract with 3L dichloromethane, wash with sodium sulfite, wash with alkali After precipitating, rectification collects 158~162 ℃ / 760mmHg distillate, obtains product weight 0.90kg, purity 99.1%, yield 91.7%.
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