72648-12-5Relevant articles and documents
Refining and purification method and drying treatment apparatus for 2-chloronicotinic acid
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Paragraph 0027; 0029; 0034; 0038; 0040; 0045; 0049; 0051, (2019/10/01)
The invention discloses a refining and purification method and a drying treatment apparatus for 2-chloronicotinic acid. The method comprises the following steps: reacting 3-methylpyridine with chlorine to produce 2-chloro-3-trichloromethylpyridine; hydrolyzing 2-chloro-3-trichloromethylpyridine to obtain a 2-chloronicotinic acid reaction product; and purifying and drying the 2-chloronicotinic acidreaction product by using the apparatus. The apparatus is applicable to drying treatment of 2-chloronicotinic acid and has a simple structure. The refining and purification method for 2-chloronicotinic acid can greatly improve the quality and purity of a 2-chloronicotinic acid product.
A 2 - chloro -5 - nitrapyrin preparation method
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Paragraph 0033-0036; 0039; 0040; 0041; 0042, (2019/03/15)
The invention discloses a 2 - chloro - 5 - trichloromethyl pyridine method, comprises the following steps: (1) the 3 - methyl pyridine is mixed with a solvent, the vaporization of the drops in the vaporization vessel, then in order to inert gas as a carrier gas, to form raw material steam; (2) dry Cl respectively2 The raw material and the steam is sent to the quartz tube catalyst [...] generating vapor phase chlorination reaction, reaction material after the condensation, rectification to obtain 2 - chloro - 5 - trichloromethyl pyridine. The invention relates to a 2 - chloro - 5 - trichloromethyl pyridine method, with raw materials are easy, low cost, easy to operate, simple process and the like.
Synthesis method of 2-chloro-trichloromethyl pyridine
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Paragraph 0022; 0025-0026; 0031; 0036; 0041; 0046; 0051, (2018/09/11)
The invention discloses a synthesis method of 2-chloro-trichloromethyl pyridine. The synthesis method comprises following steps: (1) oxidation reactions: dropwise adding an oxidizing agent into 3-trichloromethyl pyridine, and carrying out oxidation reactions at a temperature of 70 to 80 DEG C in the presence of a catalyst to obtain 3-chloromethyl pyridine oxynitride; and (2) chlorination reactions: carrying out chlorination reactions between 3-chloromethyl pyridine oxynitride obtained in the step (1) and a chlorination agent at a temperature of 20 to 25 DEG C to obtain the target product 2-chloro-trichloromethyl pyridine; wherein the solvent is an organic solvent and an organic alkali is taken as an acid-binding agent in chlorination reactions. The synthesis method is simple, the reactionconditions are mild, the yield is high, and the product purity can reach 95% or more.
PhPOCl2as a potent catalyst for chlorination reaction of phenols with PCl5
Wu, Jiang,Zhou, Junpeng,Shi, Yalei,Zhu, Jintao
supporting information, p. 1619 - 1624 (2016/10/09)
Phenols are easily converted to the corresponding aryl chlorides by using phosphorus pentachloride (PCl5) and a catalytic amount of phenylphosphonic dichloride (PhPOCl2), which is a new efficient method for synthesis of aryl chloride in good yields.
Vapor phase catalytic chlorination of ?-picoline
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Page/Page column 3-4, (2008/06/13)
2-Chloro-5-trichloromethylpyridine is obtained by chlorinating β-picoline in the vapor phase using a Mordenite zeolite or a supported palladium catalyst.