Abstract: The application provides a method for simultaneously removing oxygen-containing compounds and aromatics from high-temperature Fischer-Tropsch synthetic light oil, comprising: subjecting the light oil and a composite extractant to a countercurrent single-stage or multi-stage extraction process in an extraction equipment, to obtain a raffinate phase stream, and an extract phase stream of oxygen-containing compounds+aromatics; washing the raffinate phase stream with water, to obtain a raffinate oil stream, from which oxygen-containing compounds and aromatics have been removed, and a water stream containing a small amount of extractants; and subjecting the extract phase stream to an extractive distillation process, to obtain a recycled stream rich in alkanes and olefins and a recycled solvent-rich stream, and carrying out a regeneration cycle on the solvent-rich stream through a solvent recovery tower and a regeneration distillation tower.

Abstract: The present invention relates to technical field of chemical synthesis of drugs, and provides a preparation method of Macitentan and intermediate compound thereof. Adding THF solution containing compound II and 5-bromo-2-chloropyrimidine slowly into THF solution containing base to react, or adding THF solution containing compound II and THF solution containing 5-bromo-2-chloropyrimidine slowly at the same time into THF solution containing base to react and obtain Macitentan (shown as compound I), wherein the base is selected from sodium hydride, potassium hydride, lithium hydride or lithium bis(trimethylsilyl)amide. The selectivity of the preparation method is very good, which is suitable for industrial production. The obtained product Macitentan has good quality and high yield. And the product compound II also has good quality and high yield, its HPLC purity is up to 99.0%, the content of impurity A is less than 0.20%, the content of impurity B is less than 0.25%.

Abstract: The present invention relates to technical field of chemical synthesis of drugs, and provides a preparation method of Macitentan and intermediate compound thereof. Adding THF solution containing compound II and 5-bromo-2-chloropyrimidine slowly into THF solution containing base to react, or adding THF solution containing compound II and THF solution containing 5-bromo-2-chloropyrimidine slowly at the same time into THF solution containing base to react and obtain Macitentan (shown as compound I), wherein the base is selected from sodium hydride, potassium hydride, lithium hydride or lithium bis(trimethylsilyl)amide. The selectivity of the preparation method is very good, which is suitable for industrial production. The obtained product Macitentan has good quality and high yield. And the product compound II also has good quality and high yield, its HPLC purity is up to 99.0%, the content of impurity A is less than 0.20%, the content of impurity B is less than 0.25%.

Abstract: The present invention relates to technical field of chemical synthesis of drugs, and provides a preparation method of Macitentan and intermediate compound thereof. Adding THF solution containing compound II and 5-bromo-2-chloropyrimidine slowly into THF solution containing base to react, or adding THF solution containing compound II and THF solution containing 5-bromo-2-chloropyrimidine slowly at the same time into THF solution containing base to react and obtain Macitentan (shown as compound I), wherein the base is selected from sodium hydride, potassium hydride, lithium hydride or lithium bis(trimethylsilyl)amide. The selectivity of the preparation method is very good, which is suitable for industrial production. The obtained product Macitentan has good quality and high yield. And the product compound II also has good quality and high yield, its HPLC purity is up to 99.0%, the content of impurity A is less than 0.20%, the content of impurity B is less than 0.25%.

Abstract: A keyword extraction method is provided. In the method, a candidate keyword set in a target text is obtained by processing circuitry of a server. An extraction degree of the candidate keyword is determined by the processing circuitry based on subject similarity and a text conversion frequency of a candidate keyword in the candidate keyword set. The subject similarity is between the candidate keyword and the target text. The extraction degree indicates a probability at which the candidate keyword used as a keyword matching the target text is extracted. The keyword is extracted by the processing circuitry from the candidate keyword set according to the extraction degree.

Abstract: The present invention relates to technical field of chemical synthesis of drugs, and provides a preparation method of Macitentan and intermediate compound thereof. Adding. THF solution containing compound II and 5-bromo-2-chloropyrimidine slowly into THF solution containing base to react, or adding THF solution containing compound II and THF solution containing 5-bromo-2-chloropyrimidine slowly at the same time into THF solution containing base to react and obtain Macitentan (shown as compound I), wherein the base is selected from sodium hydride, potassium hydride, lithium hydride or lithium bis(trimethylsilyl)amide. The selectivity of the preparation method is very good, which is suitable for industrial production. The obtained product Macitentan has good quality and high yield. And the product compound II also has good quality and high yield, its HPLC purity is up to 99.0%, the content of impurity A is less than 0.20%, the content of impurity B is less than 0.25%.

Abstract: The invention relates to a method for treating oxygenated volatile organic compounds in Fischer-Tropsch synthesis reaction water. Fischer-Tropsch synthesis reaction water is subjected to (a) primary concentration and separation, (b) carbonyl compound hydrogenation, (c) carbonyl compound cutting, (d) mixed-alcohol dehydration, (e) solvent recovery, (f) ethyl alcohol separation, (g) methyl alcohol removal and separation, (h) isopropanol separation, (i) propyl alcohol cutting, (j) n-propyl alcohol separation, and (k) 2-butanol separation, so that basic organic chemicals such as ethyl alcohol, isopropanol, n-propyl alcohol, 2-butanol and mixed alcohols are obtained. Compared with the prior art, the method directly converts the concentrated Fischer-Tropsch synthesis water rich in alcohols, aldehydes, ketones, acids, and esters into a mixed-alcohol solution by hydrogenation, thus having the advantages of simple separation process and high product purity.

Abstract: A keyword extraction method is provided. In the method, a candidate keyword set in a target text is obtained by processing circuitry of a server. An extraction degree of the candidate keyword is determined by the processing circuitry based on subject similarity and a text conversion frequency of a candidate keyword in the candidate keyword set. The subject similarity is between the candidate keyword and the target text. The extraction degree indicates a probability at which the candidate keyword used as a keyword matching the target text is extracted. The keyword is extracted by the processing circuitry from the candidate keyword set according to the extraction degree.

Abstract: The present invention provides a method for preparing aniline compounds, and also provides a kind of catalyst and use thereof. This method for synthesizing an aniline compound in the invention includes following steps: use molybdenum oxide and activated carbon as catalyst, hydrazine hydrate as reducing agent, then reduce aromatic nitro compounds to aniline compounds. This method is green and high efficiency, and easy to be applied in industry.

Abstract: The present invention provides a method for preparing aniline compounds, and also provides a kind of catalyst and use thereof. This method for synthesizing an aniline compound in the invention includes following steps: use molybdenum oxide and activated carbon as catalyst, hydrazine hydrate as reducing agent, then reduce aromatic nitro compounds to aniline compounds. This method is green and high efficiency, and easy to be applied in industry.