Process for synthesizing 2, 3, 3, 3-tetrafluoropropionic acid
A synthesis method and technology of tetrafluoropropionic acid, applied in the directions of organic chemistry, amide preparation, etc., can solve the problems of increasing the difficulty and cost of waste liquid treatment in factories, many by-product impurities, difficult reaction control, etc., and achieve low price and rapid reaction. , Easy to operate effect
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Embodiment 1
[0021] Add 201 g (1.0 mol) of N,N-diethyl-2,3,3,3-tetrafluoropropionamide, 100 g of concentrated sulfuric acid (98%), 16 g of water, and 10.05 g of copper sulfate into the three-necked flask, and stir to raise the temperature The temperature was 120°C, and the reaction was carried out for 6 hours. TLC detected that the reaction was complete, and fractional distillation was started to obtain 140 g of the product with a GC content of 99.6% and a molar yield of 96%.
Embodiment 2
[0023] Add 201 grams (1.0mol) of N,N-diethyl-2,3,3,3-tetrafluoropropionamide, 2147 grams of 17% hydrochloric acid aqueous solution and 2.01 grams of copper chloride into the three-necked flask, stir and heat up to 40 ℃, reacted for 30 hours, TLC detected that the reaction was complete, and started fractional distillation to obtain 132 g of the product with a GC content of 99.2% and a molar yield of 91%.
Embodiment 3
[0025] Add 201 grams (1.0mol) of N,N-diethyl-2,3,3,3-tetrafluoropropionamide, 2010 grams of 40% trifluoroacetic acid aqueous solution and 5 grams of ferrous chloride into the three-necked flask, and stir The temperature was raised to 75°C, and the reaction was maintained for 20 hours. TLC detected that the reaction was complete, and fractional distillation was started to obtain 132 grams of the product with a GC content of 99.1% and a molar yield of 91%.
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