34 results about "Chloracetone" patented technology

The invention provides a method for preparing deuterated chloroform by using hexachloroacetone as an intermediate. The method comprises the following steps: step 1, producing hexachloroacetone by monochloroacetone and / or polychlorinated acetone raw material liquid, and comprising the steps of raw material liquid pre-treatment, chlorination catalytic reaction and reaction product purification; step 2, producing deuterated chloroform by taking hexachloroacetone as raw material, and comprising the steps of hydrolytic catalytic reaction and reaction product purification. The method solves the problem of the disposing of waste material produced during the production of monochloroacetone, trichloroacetone and the like, and is in favor of relieving the environment burden; common cheap chemical is used as catalytic agent, the side reaction is less, the reaction product is easy to separate, and the content of the produced pollutant is greatly lowered. Through the utilization of the polarization and weakening effects of connecting bond of the carbonyl carbon of the hexachloroacetone and trichloromethyl, the carbonyl carbon of the hexachloroacetone and trichloromethyl are hydrolyzed in an alkalescence condition to produce deuterated chloroform, and the reaction product is CO2 that can be discharged into air directly. The method has important social benefits and economic benefits.

The present invention relates to a kind of synthetic method of 2-methyl-3-hydroxyquinoline and the preparation method of quinone disperse dye; in the synthetic method of 2-methyl-3-hydroxyquinoline, first anthranil , chloroacetone, alkali catalyst, phase transfer catalyst and solvent are mixed, and the pH value is adjusted to 11-13. Under the action of the phase transfer catalyst, each raw material is fully contacted to obtain a uniformly mixed homogeneous mixed solution with a specific pH value; Then the mixed solution is subjected to a microchannel reaction. During the microchannel reaction, the reaction materials in the mixed solution can undergo micron or millimeter level micro-contact reactions, which improves the reaction speed and reaction selectivity, and reduces the amount of ortho-amino groups in the microchannel reaction process. The possibility of benzaldehyde or chloroacetone undergoing self-condensation, thereby improving the yield of 2-methyl-3-hydroxyquinoline.

The invention discloses a method for preparing pymetrozine with an aim to provide a synthesis method short in reaction route of the pymetrozine, small in environmental pollution and simple in technology operation, and belongs to the technical field of organic synthesis. The method includes the steps of 1), allowing dimethyl carbonate serving as a raw material to be subjected to hydrazinolysis withhydrazine hydrate to obtain carbazide; 2), subjecting carbazide and smoke aldehyde to condensation reaction to obtain (E)-N'-(pyridine-3-kiya methyl) hydrazine carbon hydrazide; 3), subjecting (E)-N'-( pyridine-3-kiya methyl) hydrazine carbon hydrazide and chloroacetone to condensation reaction to obtain (E)-N'-(Z)-1-chloropropyl-2-subunit)-2-(pyridine-3-kiya methyl) diazanyl-1-carbohydrazide; 4), subjecting (E)-N'-(Z)-1-chloropropyl-2-subunit)-2-(pyridine-3-kiya methyl) diazanyl-1-carbohydrazide to ring formation under the alkaline condition to obtain the pymetrozine.

The invention relates to a simple synthesis method of a 2-aminothiophene derivative. The method comprises the steps of condensating monochloroacetone, alkyl / aryl-piperzine under the effect of inorganic base to prepare a piperzine derivative II, mixing the piperzine derivative II with 4-chlorobenzoyl acetonitrile and sulphur, dropping organic amine, performing heat preservation reaction, and reacting in two steps to obtain 2-amino-3,(4- chlorine)-benzoyl-4-(N- alkyl / aryl-piperzine-N '-) methylthiophene. The simple synthesis method of the 2-aminothiophene derivative is available in raw materials, simple to operate, simple in synthesis steps and environmental-friendly; meanwhile, products are high in selectivity, yield and purity and applicable to industrial application.

The invention relates to a preparation method of hexachloroacetone, which belongs to the technical field of organic chemical gas preparation. Compound A and chlorine molecule B are mixed and reacted at 30°C to 150°C under the action of a catalyst, and the reaction product is a mixture containing hexachloroacetone and the catalyst; the catalyst is separated from the mixture to obtain a crude product; the crude product is purified to obtain Hexachloroacetone; compound A is at least one of acetone and chloroacetone with chlorine atoms of 1 to 5; chlorine molecule B is a mixture of chlorine or chlorine and a diluent gas, and the diluent gas is an inert gas or nitrogen; the catalyst is pyrimidine, 2-chloropyrimidine, 2-cyanopyrimidine or s-triazine. The method is easy to recover the catalyst, and can obtain the hexachloroacetone with extremely low impurity content in high yield.

The invention discloses a method for purifying high-purity trichloroacetone for preparation of folic acid. The method is characterized in that a water solvent is used for purifying to prepare the high-purity trichloroacetone, and comprises the following steps of step 1, using the water solvent to extract the trichloroacetone with purity of 50% by three times; step 2, recrystallizing the obtained extracting solution by a gradient cooling type, and increasing the purity of the crude trichloroacetone with purity of about 50% to be above 98% by two steps of purification, wherein the extracting yield rate of trichloroacetone is 90% or above, the solution after separating and crystallizing in step 2 can be repeatedly utilized, and the yield rate of trichloroacetone can reach 80% or above by raw material. The method has the advantages that the preparation of high-purity trichloroacetone is easy, the safety and environment-friendly effects are realized, and the requirement of industrialization on environment protection is met; the prepared high-purity trichloroacetone can be used for preparing the folic acid, and the yield rate and purity of the folic acid are certainly improved.

The invention discloses a hydrodechlorination device and method for trichloroacetone, relates to the technical field of chemical purification, and comprises a reaction vessel and a base, the reaction vessel is placed above the base, and the reaction vessel is provided with a first bottle opening, The second bottleneck, the third bottleneck and the fourth bottleneck, the second bottleneck is located at the center position, and a stirring structure is arranged in the second bottleneck; the stirring mechanism includes a stirring rod, a stirring rod arranged on the outside The end cover plug, the sliding sleeve, the stirring blade arranged at the bottom of the stirring rod and the connecting rod rotatably connected with the stirring blade, the feeding structure is arranged inside the stirring rod, and the upper end of the stirring rod is connected with the driving mechanism. This invention eliminates the The magnetic stirring bar interferes with the tubes in the reaction vessel when rotating, and improves the stirring efficiency at the same time, which is suitable for batch dechlorination treatment; and the stirring blades are easy to extend and retract, which is convenient for installation and disassembly.