908009-54-1Relevant articles and documents
Method for efficient synthesis of 2-chloro-4-fluoro-5-nitrotrichlorotoluene
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Paragraph 0023-0046, (2019/02/10)
The invention discloses a method for efficient synthesis of 2-chloro-4-fluoro-5-nitrotrichlorotoluene. The method comprises the following steps of (1) a nitrification reaction, wherein concentration sulfuric acid with the mass concentration of 98% and concentrated nitric acid with the mass concentration of 98 % are mixed according to the mass ratio of 1:1 to prepare mixed acid, and 2-chloro-4-fluorotrichlorotoluene is added dropwise into the mixed acid under the condition of stirring to carry out the nitration reaction; (2) quenching of the reaction, wherein a nitrified material obtained afterthe nitrification reaction is put into an ice-water mixture for stirring to quench the reaction; (3) preparation of a dry product, wherein after the reaction is quenched, a circulating water vacuum pump is adopted for suction filtration, and then washing and drying are conducted to obtain the dry product of 2-chloro-4-fluoro-5-nitrotrichlorotoluene; (4) recycling, wherein a filtrate obtained after the suction filtration and washing water are recovered for recycling. The method can improve the production efficiency, the color of the finished product is pure, and the yield and purity of the product are also high and are both 90% or above.
PROCESS FOR THE PREPARATION OF 2-CHLORO-4-FLUORO-5-NITROBENZOTRICHLORIDE
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Page/Page column 6; 7; 8, (2018/08/26)
The present invention relates to an improved process for the preparation of 2-chloro-4-fluoro-5-nitrobenzotrichloride. The present invention further relates to a process for the purification of 2-chloro-4-fluoro-5-nitrobenzotrichloride, which reduces the isomeric impurities and acidic by-products.
PROCESS FOR THE PREPARATION OF BENZOIC ACID DERIVATIVES VIA A NEW INTERMEDIATE OF SYNTHESIS
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Page/Page column 5-6, (2009/06/27)
The object of the invention is the preparation of 2-chloro-4-fluoro-5-nitrobenzoic acid and derivatives thereof, by nitration of 2-chloro-4-fuorobenzotrichloride and the conversion of the novel synthetic intermediate thus obtained into its acid form or de