Method for preparing 2, 4-dichloroacetophenone
A technology of dichloroacetophenone and production method, applied in the direction of condensation preparation of carbonyl compounds, organic chemistry, etc., can solve problems such as explosion, harsh requirements, fire, etc., to reduce production costs, improve intrinsic safety, and realize comprehensive utilization Effect
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[0011] Add 1.0mol m-dichlorobenzene and 1.3mol anhydrous aluminum trichloride to the reaction kettle, slowly add 1.0mol acetic anhydride dropwise under stirring, the temperature of the reaction solution is kept at 45°C-55°C during the dropwise addition, and the dropwise Heat up to 90~95°C at a rate of 1°C / min, reflux and stir for about 3 hours. After the reaction, add 200ml of 10% hydrochloric acid to the reaction solution and hydrolyze at 80°C. Leave it to cool and separate layers, separate the organic layer, drop Add it to a washing kettle with 200ml of water and wash it with water at 50°C. After standing and stratifying, the product is distilled under reduced pressure at 120-140°C, and the fraction before 135°C is collected, cooled and crystallized to obtain a white crystal with a purity of more than 99%. 4-Dichloroacetophenone.
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