1926 results about "Methyl benzene" patented technology

The present invention discloses a method for detecting and applying C1-C2-alkyl-substituted phenol isomers, which relates to the technical field of environmental detection and includes: selecting a corresponding sample pretreatment process to prepare a test sample according to the petroleum content range in the sample; under a mobile phase of methanol-5.0-6.5 mmol / L ammonia water, using LC-MS to detect the test sample to obtain the concentration of the first component and the standardized concentrations of co-eluted 3,5-dimethylphenol and 2,6-dimethylphenol; under a mobile phase of acetonitrile-4.0-10.0 mmol / L ammonia water, using LC-MS to detect the test sample to obtain the concentration of 3,5-dimethylphenol, or the standardized concentrations of co-eluted 3,5-methylphenol and 3-ethylphenol, or the standardized concentrations of co-eluted 2,6-dimethylphenol and 2,4-dimethylphenol; under a mobile phase of methanol-5.0-6.5 mmol / L ammonia water or acetonitrile-4.0-10.0 mmol / L ammonia water, using LC-MS to separately detect the calibration samples of the co-eluted components, and calculate the conversion factor of the co-eluted components and the concentration of the other component. The present invention realizes the accurate quantification of phenol and 12 C1-C2-alkyl-substituted phenol isomers.

The present invention discloses a characterization method and application of C0-C2-alkyl-substituted phenols, relating to the technical field of environmental detection. The method includes: selecting a corresponding sample pretreatment process to prepare a test sample according to the petroleum content range in the sample; detecting the test sample by LC-MS under a mobile phase system of methanol-5.0-6.5 mmol / L ammonia water to obtain the concentration of the first component and the normalized concentrations of co-eluted 3,5-dimethylphenol and 2,6-dimethylphenol; detecting the test sample by LC-MS under a mobile phase system of methanol-7.0-11.5 mmol / L ammonia water to obtain the concentration of 3,5-dimethylphenol; detecting calibration samples of 3,5-dimethylphenol and 2,6-dimethylphenol respectively by LC-MS under a mobile phase system of methanol-5.0-6.5 mmol / L ammonia water, calculating a conversion factor, and obtaining the concentration of 2,6-dimethylphenol; and obtaining the contents of 13 single components of C0-C2-alkyl-substituted phenols based on the concentrations of the first component, 3,5-dimethylphenol and 2,6-dimethylphenol. The present invention realizes the quantitative characterization of 13 single components of C0-C2-alkyl-substituted phenols.

The invention discloses a preparation method of a GLP-1R agonist Orforglipron, which comprises the following reaction steps: carrying out four-step reaction on an oxopiperidine compound (1) and (4-fluoro-3, 5-dimethylphenyl) hydrazine (2) to obtain a compound 8, and carrying out seven-step reaction on 5-bromo-indolecarboxylic acid (9) to obtain a compound 17. Then, the compound 8 and a compound 17 are subjected to an acid amine condensation reaction, and Orforglipron (LY3502970) is obtained. The preparation method is relatively low in cost, easy to operate, relatively short in synthetic route and suitable for industrial production and application, and the total yield can reach 32%.

The present disclosure relates with the development of a process for producing gels from polymeric materials crosslinked with organic agents and their use controlling water in porous media under high salinity and temperature conditions. The characteristics of these gels enable them to have a good performance withstanding extreme conditions in mature Mexican oil wells and in others located in other parts of the world. The gels featured in the present disclosure include novel ionic terpolymers based on acrylamide (AM), N-vinylpyrrolidone (VP), N,N′-methylenebisacrylamide (BAA), 1-vinyl-3-butylimidazolium bromide (VIM4C[Br]) and organic crosslinking agents.

The invention discloses unsaturated polyester resin for an unmanned aerial vehicle fuselage and a preparation method of the unsaturated polyester resin, and relates to the field of high polymer materials. When the unsaturated polyester resin for the unmanned aerial vehicle fuselage is prepared, a flame-retardant monomer reacts with 2-hydroxy-5-(hydroxymethyl) benzaldehyde to prepare a modified flame-retardant monomer; reacting cellulose with acrylic acid to obtain pre-modified cellulose; the pre-modified cellulose, 1-allyl-1, 1, 3, 3-tetramethyldisiloxane and chloroplatinic acid are subjected to a reaction, and modified cellulose is prepared; maleic anhydride, 5-(1H-imidazole-1-yl)-1, 3-phthalic acid, propylene glycol and the modified flame-retardant monomer are subjected to a reaction, and pre-polyester is prepared; and stirring the pre-polyester, zinc chloride, modified cellulose, benzophenone peroxide and styrene to obtain the anti-aging coating. The prepared unsaturated polyester resin for the unmanned aerial vehicle fuselage has good anti-aging, self-repairing, flame-retardant and self-cleaning performance.

The invention relates to a phosphorus-free zinc-free seawater special-purpose scale and corrosion inhibitor, which comprises, by weight, 20-25% of sulfonic acid modified polyaspartic acid, 8-12% of quaternized chitosan, 5-10% of a sulfonate copolymer, 5-10% of polyepoxysuccinic acid, 1-3% of benzotriazole or methyl benzotriazole, 0.5-1% of sodium tungstate, and the balance of deionized water. According to the formula, traditional corrosion inhibitors such as phosphorus and zinc are completely abandoned, functions are achieved through natural polymer derivatives such as sulfonic acid modified polyaspartic acid and quaternized chitosan, and the scale and corrosion inhibitor has the following environmental protection advantages that the scale and corrosion inhibitor does not contain phosphorus and zinc elements at all, and water eutrophication and heavy metal accumulation caused by a traditional phosphorus and zinc formula are avoided.

A disulfiram derivative of formula (I)wherein R1 and R2 are independently —CH2CH2COOH, —CH2CH2COOEt, optionally substituted methylenepyridyl, optionally substituted methylenefuranyl, or optionally substituted methylenethiopenyl, may be useful in aldehyde dehydrogenase 1a1 (ALDH1a1) and / or monoacylglycerol lipase (MAGL)-mediated diseases or disorders. Such derivatives may avoid or limit aldehyde dehydrogenase 2 (ALDH2) and / or fatty acid amide hydrolase (FAAH) antagonism.

The invention discloses a quick-curing polyurethane seamless expansion joint material for roads and a preparation method, and belongs to the technical field of road engineering materials. The material is prepared from polyether polyol, polycaprolactone glycol, a bisphenol A epoxy-polyether block isocyanate terminated prepolymer, a methyl phenyl silicon-boron hybrid hydroxyl chain extender, diphenylmethane diisocyanate, calcium carbonate, wollastonite, a hindered amine anti-aging agent and dioctyl phthalate. Wherein the bisphenol A epoxy-polyether block isocyanate terminated prepolymer is prepared by the following steps: reacting bisphenol A with epoxy chloropropane to generate epoxy resin, reacting with polytetramethylene ether glycol, and introducing isophorone diisocyanate; the methyl phenyl silicon-boron hybrid hydroxyl chain extender is prepared by carrying out hydrosilylation and ethylene glycol reaction on methyl trimethoxy silane, 3-glycidyl ether oxypropyl trimethoxy silane and allylboronic acid pinacol ester; and the methyl phenyl silicon-boron hybrid hydroxyl chain extender is prepared by carrying out hydrosilylation on methyl trimethoxy silane, 3-glycidyl ether oxypropyl trimethoxy silane and allylboronic acid pinacol ester. The material has the advantages of quick curing property, weather resistance and high-temperature stability, and is suitable for road seamless expansion joint scenes.

The present invention relates to a method for the synthesis of a carboxylic diacid, having a 5- or 6-membered heteroaromatic compound optionally comprising an allyl or methylstyrene function, preferably selected from 5- or 6-membered heteroaromatic compounds and comprising at least one heteroatom selected from nitrogen, sulphur and oxygen.

The invention provides a preparation method of 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride, which comprises the following steps: salifying 4-fluoro-3, 5-dimethylaniline serving as a substrate with concentrated hydrochloric acid, reacting with sodium nitrite to prepare a diazo solution, reducing the diazo solution into corresponding phenylhydrazine by using alkaline sodium sulfite as a reducing agent system, and reacting the 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride with the diazo solution to prepare the 4-fluoro-3, 5-dimethylphenylhydrazine hydrochloride. And acidizing the 2, 5-dimethyl phenylhydrazine to obtain corresponding phenylhydrazine hydrochloride. According to the preparation method, sodium sulfite which is low in cost and easy to obtain is used as a reducing agent, the defects that metal residues are high, the environment is prone to being polluted and the raw material cost is high due to the fact that a metal reducing agent is adopted when phenylhydrazine hydrochloride is prepared in the prior art are overcome, the reaction is completed in a water phase, no organic solvent is adopted, and the concept of green chemistry is met; and the problems of complicated post-treatment and easy pollution caused by the adoption of an organic solvent can be effectively avoided.

The invention relates to an electric heating type liquid crystal elastomer artificial muscle and a preparation method thereof, belongs to the technical field of intelligent high polymer materials, and solves the technical problems that the liquid crystal elastomer artificial muscle in the prior art is easy to harden and embrittle due to excessive filler and is weak in deformability. The electric heating type liquid crystal elastomer artificial muscle comprises two layers of liquid crystal elastomer films and an electric heating element, the electric heating element is arranged between the two layers of liquid crystal elastomer films; the raw materials of the liquid crystal elastomer film comprise a liquid crystal unit, a chain extender, a cross-linking agent and a catalyst. Wherein the liquid crystal unit is 1, 4-bis-[4-(3-acryloyloxy propoxy) benzoyloxy]-2-methyl benzene. Joule heat generated by the electric heating element can activate the liquid crystal elastomer, deformation of the liquid crystal elastomer is not limited, and therefore the liquid crystal elastomer has the advantages of being high in deformability, controllable in heating mode and time, programmable in driving and the like; and a self-sensing function is also realized, and the shape change can be monitored and regulated in real time according to the resistance.

An active energy ray-curable inkjet printing ink composition satisfies requirements A to E below is provided: (A) the content of amine-modified oligomer is 1.0 to 20.0% by mass; (B) alkoxy group-containing (meth)acrylate monomers are contained by 2.0 to 20.0% by mass; (C) (meth)acrylate monomers having an alkyl group with 6 to 20 carbon atoms is contained by 2.0 to 25.0% by mass; (D) at least one type selected from the group that consists of 1,6-hexanediol diacrylate, 3-methyl-1,5-pentanediol diacrylate, dipropylene glycol diacrylate, 1,10-decanediol diacrylate, propoxylated(2)neopentyl glycol diacrylate, and hydroxypivalic acid neopentyl glycol diacrylate is contained by 30.0 to 60.0% by mass; (E) as photopolymerization initiators, ethoxy(2,4,6-trimethylbenzoyl)phenylphosphine oxide is contained by 3.0 to 15.0% by, and oligo(2-hydroxy-2-methyl-1-(4-(1-methylvinyl)phenyl)propanone) and / or 2-hydroxy-1-{4-[4-(2-hydroxy-2-methylpropionyl)phenoxy]phenyl}-2-methylpropanone is / are contained by 2.0 to 10.0% by mass, where the total content of photopolymerization initiators is 6.0 to 25.0% by mass.

The invention relates to the field of catalysts, and discloses a hydrogenation catalyst, a preparation method and application thereof, and a method for preparing alpha-methylbenzyl alcohol, the hydrogenation catalyst comprises a hydrogenation active component and a SiO2 carrier; the surface of the catalyst is modified by siloxane groups. The hydrogenation catalyst has the characteristics of high low-temperature hydrogenation activity and long service life. The hydrogenation catalyst is used in a liquid phase hydrogenation reaction and has high catalytic activity, so that a low-temperature liquid phase reaction can be better carried out, for example, the hydrogenation catalyst is used in preparation of alpha-methylbenzyl alcohol, the raw material acetophenone can obtain a high conversion rate, the alpha-methylbenzyl alcohol has high selectivity, and meanwhile, the hydrogenation catalyst is long in service life.

The invention relates to the technical field of water treatment, in particular to a reverse osmosis membrane and a preparation method thereof. The preparation method of the reverse osmosis membrane comprises the following steps: soaking a base membrane in a water phase solution, taking out the base membrane, drying the surface of the base membrane, coating the base membrane with an oil phase solution, carrying out interfacial polymerization reaction, curing, coating with a modifier solution, and drying to obtain the reverse osmosis membrane, the modifying agent comprises 2, 4, 6-tri (4-aminophenyl)-1, 3, 5-triazine-1, 3, 5-tri (4-methyl phenyl) benzene. The successfully grafted COFs can improve the water permeability of the membrane to a certain extent, and also can improve the pollution resistance, acid resistance and oxidation resistance of the membrane, so that the service life of the membrane is prolonged. According to the invention, different effects of the same type of imino COFs introduced to the reverse osmosis membrane are further compared, so that the excellence of the selected imino COFs is highlighted.

The invention discloses a gamma-aminobutyric acid gated chloride ion channel allosteric modifier compound and an application thereof, namely (S)-4-(5-(3-chloro-5-(trifluoromethyl) phenyl)-5-(trifluoromethyl)-4, 5-dihydroisoxazole-3-yl)-2-methyl-N-(2-oxo-2-((2, 2, 2-trifluoroethyl) amino) ethyl) benzamide, and a preparation method of the gamma-aminobutyric acid gated chloride ion channel allosteric modifier compound. The compound has an excellent control effect on pests of thysanoptera, acarina, lepidoptera and the like, is very friendly to bees and high in environmental ecological safety, can be used for preparing efficient, low-toxicity and safe insecticides, and has a wide application prospect in agricultural production.

The present invention relates to the field of water treatment technology, and more particularly to a kind of reverse osmosis membrane and preparation method thereof.The preparation method of the reverse osmosis membrane includes:Basement membrane is soaked in aqueous phase solution, after taking out surface drying, oil phase solution is coated on basement membrane and carries out interfacial polymerization reaction, after solidification, coating modifier solution, after drying, obtain reverse osmosis membrane;The modifier includes 2,4,6-tris (4-aminophenyl) ‑1,3,5-triazine ‑1,3,5-tris (4-methylphenyl) benzene.The COFs successfully grafted by the present invention can improve the water permeability of membrane to a certain extent, and can also improve the anti-pollution property, acid resistance and oxidation resistance of membrane, and then improve the service life of membrane.The present invention further compares the different effects that the same type of imino COFs are introduced into reverse osmosis membrane, so as to highlight the excellence of the imino COFs selected by the present invention.

The invention relates to the field of fire-resistant oil, in particular to phosphate-based fire-resistant oil with synergistically optimized flame resistance and stability and a preparation method of the phosphate-based fire-resistant oil. The fire-resistant oil comprises base oil and an additive, the base oil is a mixture obtained by esterification of mixed alkylphenol and phosphorus oxychloride; the molar percentage of the mixed alkylphenol is as follows: 4-6% of phenol; 11 to 14 percent of p-methylphenol; 22 to 26 percent of 2, 5-position dimethyl phenol; 0.8 to 1.5 percent of 2, 4-position dimethyl phenol; 2.5 to 4 percent of 2, 3-position dimethyl phenol; 0.4 to 0.6 percent of 4-ethyl phenol; 40 to 48 percent of 3, 5-position dimethyl phenol; 8 to 11% of 3-ethyl phenol; 3 to 5 percent of 3, 4-position dimethyl phenol; the additives comprise an antioxidant, a corrosion inhibitor, an anti-foaming agent and an anti-hydrolysis agent; the addition amount of the antioxidant is 0.05-5% of the total mass of the base oil; the addition amount of the corrosion inhibitor is 0.001%-0.08% of the total mass of the base oil; the addition amount of the anti-foaming agent is 0.001%-0.009% of the total mass of the base oil; the addition amount of the anti-hydrolysis agent is 0.001%-0.005% of the total mass of the base oil. The fire-resistant oil provided by the invention can be safely used under the working conditions of high temperature and extreme pressure.

The invention relates to a TSV (through silicon via)-based copper / titanium / TEOS (tetraethyl orthosilicate) rate selective control CMP (chemical mechanical polishing) solution. The polishing solution is prepared from nanoscale silicon dioxide, a complexing agent, an inhibitor, a surfactant, an oxidizing agent and deionized water, the pH value of the alkaline polishing solution is 8.0; the invention discloses a polishing solution. 2, 2 '-[[((methyl-1H-benzotriazole-1-yl) methyl] imino] diethanol (TT-LYK) and octyl hydroxamic acid (OHA) are used as inhibitors, the two inhibitors act independently or are compounded, and under the synergistic effect of the inhibitors and the complexing agent, the polishing solution has the high polishing rate and the good surface quality performance, meanwhile, the rate of copper / titanium / TEOS can be selectively controlled, and the polishing effect is good. And dish-shaped recesses and dielectric layer erosion after polishing are improved. The polishing solution prepared by the invention is simple in preparation process and easy for large-scale production, and meets the actual requirements of industrial application.

The invention relates to a preparation method of 3-[(1S, 2S)-1-[5-[(4S)-2, 2-dimethyl oxacyclohexane-4-yl]-2-[(4S)-2-(4-fluoro-3, 5-dimethyl phenyl)-3-[3-(4-fluoro-1-methylindazol-5-yl)-2-oxoimidazol-1-yl]-4-methyl-6, 7-dihydro-4H-pyrazolo [4, 3-c] pyridine-5-carbonyl] indol-1-yl]-2-methylcyclopropyl]-4H-1, 2, 3-triazolo [4, 3-c] pyridine-5-carbonyl] indol-1-yl]-2-methylcyclopropyl]-1, 2, 4-triazolo [4, 3-c] pyridine-5- The invention relates to synthesis of 1, 2, 4-oxadiazole-5-one or a salt thereof, and related synthesis intermediate compounds.

The present invention relates to a liquid pharmaceutical composition suitable for administration by inhalation comprising: (i) a suspension of particles comprising 9,10-dimethoxy-2-(2,4,6-trimethylphenylimino)-3-(N-carbamoyl-2-aminoethyl)-3,4,6,7-tetrahydro-2H-pyrimido[6,1-a]isoquinolin-4-one (RPL554); and (ii) a diluent which is 1,1,1,2-tetrafluoroethane (HFA-134a), wherein the liquid pharmaceutical composition is substantially free of surfactant. The invention also relates to a pressurised metered dose inhaler comprising the liquid pharmaceutical composition.

The invention relates to the field of water treatment, and discloses a scale and corrosion inhibitor for seawater circulating cooling water, which is prepared from phosphonic acid grafted maleic anhydride-acrylic acid copolymer, hydroxyethylidene diphosphonic acid, amino trimethylene phosphonic acid, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N- The anti-corrosion coating is prepared from the following raw materials: N, N-diethylaminomethyl-benzotriazole, gamma-aminopropyltriethoxysilane, zinc salt and a polyoxyethylene-polyoxypropylene block copolymer. The core of the invention is that all the raw material components form the thermo-sensitive polyelectrolyte compound through a self-assembly process. The compound is stably dispersed at low temperature by utilizing the cloud point effect of the block copolymer, and is subjected to phase change and preferential deposition on a high-temperature heat exchange surface, so that targeted and efficient delivery of various active components is realized. According to the invention, the problems of incompatibility of components and poor stability of a traditional compound agent are solved, the product has excellent storage stability, and efficient and synergistic corrosion and scaling control can be realized under high-temperature and high-salinity working conditions.

The invention discloses a continuous reaction device and method for producing 2-amino-4-methylbenzothiazole, and belongs to the technical field of compound production. The invention relates to a continuous reaction device for producing 2-amino-4-methylbenzothiazole, which comprises a first-stage reaction kettle and further comprises a stirring mechanism arranged in the first-stage reaction kettle and used for stirring chlorine and a mixed solution in the first-stage reaction kettle; the driving mechanism is arranged at the top of the first-stage reaction kettle and is used for driving the stirring mechanism to perform stirring action in the first-stage reaction kettle; the chlorine injection mechanism is connected with the stirring mechanism; the air exhaust mechanism is arranged at the top of the first-stage reaction kettle and is connected with the driving mechanism; the multistage reaction kettles are adopted for continuous operation to eliminate downtime, so that the problem of low production efficiency caused by repeated heating and cooling due to the use of intermittent reaction kettles in the traditional process is solved, the chlorine utilization rate is improved, and the production and processing cost is effectively reduced.

The invention belongs to the technical field of medicinal chemistry, and particularly relates to a preparation method and application of N-(3-chloro-4-fluorophenyl)-4-fluoro-3, 5-dimethyl benzenesulfonamide and analogues thereof, and a medicinal composition of the N-(3-chloro-4-fluorophenyl)-4-fluoro-3, 5-dimethyl benzenesulfonamide and the analogues thereof. The method comprises the following steps: dissolving a compound 1 and a compound 2 in an organic solvent, adding an acid-binding agent, carrying out a stirring reaction at 20-100 DEG C, and carrying out TLC detection until raw material fluorescence disappears so as to complete the reaction; and carrying out spin-drying on the reaction liquid, and carrying out crystallization or column chromatography separation on a crude product to obtain N-(3-chloro-4-fluorophenyl)-4-fluoro-3, 5-dimethyl benzenesulfonamide and the analogue of N-(3-chloro-4-fluorophenyl)-4-fluoro-3, 5-dimethyl benzenesulfonamide. N-(3-chloro-4-fluorophenyl)-4-fluoro-3, 5-dimethylbenzenesulfonamide and analogues thereof are used for recovering the physiological level of TERT in senescent tissues, and N-(3-chloro-4-fluorophenyl)-4-fluoro-3, 5-dimethylbenzenesulfonamide and analogues thereof are used for preparing oral pharmaceutical compositions. The N-(3-chloro-4-fluorophenyl)-4-fluoro-3, 5-dimethylbenzenesulfonamide and the analogue thereof can be used for recovering the physiological level of TERT (telomerase reverse transcriptase) of the whole aging tissue and relieving various aging characteristics.

The present invention relates to the synthesis of 3-[(1S,2S)-1-[5-[(4S)-2,2-dimethyloxan-4-yl]-2-[(4S)-2-(4-fluoro-3,5-dimethylphenyl)-3-[3-(4-fluoro-1-methylindazol-5-yl)-2-oxoimidazol-1-yl]-4-methyl-6,7-dihydro-4H-pyrazolo [4,3-c] pyridine-5-carbonyl] indol-1-yl]-2-methylcyclopropyl]-4H-1,2,4-oxadiazol-5-one, or a salt thereof, and related synthetic intermediate compounds.

The invention relates to the technical field of bioanalytical chemistry, in particular to a method for simultaneously enriching and separating glycopeptides and phosphopeptides by using a bionic hydrophilic adsorbent, which specifically comprises the following steps: step 1, preparing a polyether-ether-ketone (PEEK) framework by using a fused deposition modeling method (FDM); 2, soaking the obtained PEEK framework in an aqueous solution containing dopamine hydrochloride and tris (hydroxymethyl) aminomethane, and carrying out a reaction; step 3, then, adding a mixed solution containing hyaluronic acid methacrylate, vinyl phosphoric acid, N, N-dimethyl bisacrylamide and phenyl-2, 4, 6-trimethylbenzoyl lithium phosphate into the PEEK framework; in the invention, in the aspect of material preparation, a fused deposition modeling method (FDM) is adopted to prepare a polyether-ether-ketone (PEEK) frame, and the material has good mechanical properties and chemical stability and can bear a series of subsequent complex treatment processes without being damaged.

The invention relates to the field of sealing materials, in particular to a butyl rubber sealing material and a preparation method thereof. Comprising the following components in parts by weight: 50-70 parts of butyl rubber, 30-50 parts of a brominated isobutylene-p-methylstyrene copolymer, 30-50 parts of carbon black, 8-12 parts of an alkyl phenolic resin vulcanizing agent, 3-5 parts of zinc oxide, 1-3 parts of stearic acid, 1-3 parts of an anti-aging agent and 5-10 parts of a plasticizer. The butyl rubber provides ideal air tightness and heat aging resistance, bromine atoms are introduced into the brominated isobutylene-p-methylstyrene copolymer, co-vulcanization with the butyl rubber is achieved, it is ensured that a uniform and stable co-crosslinking network can be formed between the two rubber molecules, and the service life of the rubber is prolonged. The alkyl phenolic resin vulcanizing agent can form a C-C bond with high bond energy with two rubber molecules, so that the thermal aging resistance of the butyl rubber sealing material is effectively improved, the compression set is reduced, and the butyl rubber sealing material with excellent performance is prepared.

The present invention relates to the technical field of mold release agents, and specifically discloses a mold release agent for the integrated die-casting of aluminum alloy automobiles, which comprises the following raw materials in parts by weight: 15-20 parts of fluorinated wax emulsion, 6-8 parts of sodium dodecylbenzenesulfonate, 3-6 parts of Tween 80, 3-5 parts of methylphenyl modified silicone oil, 4-6 parts of graphene regulator, 2-4 parts of nano-silica modifier, 2-4 parts of silane coupling agent, and 10-15 parts of water. The mold release agent of the present invention uses fluorinated wax emulsion in combination with sodium dodecylbenzenesulfonate, Tween 80, and methylphenyl modified silicone as the matrix materials, and through the addition of graphene regulator, nano-silica modifier, and silane coupling agent to coordinate with each other and work together synergistically, with the silane coupling agent as the interfacial agent to enhance the interfacial effect between the raw materials of the system.

The invention relates to a method for synthesizing trifloxystrobin through a one-pot method, and belongs to the technical field of organic synthesis.The method comprises the following steps that 1, E-2-(2-halomethylphenyl)-2-methoxyiminoacetic acid methyl ester, m-trifluoromethyl acetophenone, hydroxylamine hydrochloride or hydroxylamine sulfate and a solvent are added into a reaction flask, then alkali is added, and after addition is completed, a heat preservation reaction is conducted; and Step 2, after the reaction is finished, filtering to remove salt, and concentrating filtrate under reduced pressure to obtain trifloxystrobin. Compared with a traditional synthesis method of the trifloxystrobin, the synthesis method of the trifloxystrobin has the advantages that the 3-trifluoromethyl acetophenone and the E-2-(2-halomethylphenyl)-2-methoxyiminoacetic acid methyl ester are used as raw materials, the trifloxystrobin is directly synthesized by a one-pot method, the reaction route is short, the raw material cost is low, and the synthesis method of the trifloxystrobin by the one-pot method has the advantages that the synthesis efficiency is high, and the synthesis cost is low. The preparation method has the advantages that the preparation of m-trifluoromethyl acetophenone oxime from m-trifluoromethyl acetophenone is not needed, the whole synthesis process is simpler and more efficient, the reaction conditions are mild, and the preparation method is suitable for industrial large-scale production.

The invention discloses a potassium-free catalyst and method for preparing p-methylstyrene with a low water-hydrocarbon ratio, the catalyst takes Fe-modified gamma-Al2O3 prepared by an oil column forming method as a carrier, and active metal and auxiliary metal are loaded through autoclave crystallization. Transition metal Fe is introduced in the technological process of preparing the gamma-Al2O3 carrier through a hot oil column forming method, after other metal salts are dissolved in an acid solution, polyethylene glycol and citric acid are added to serve as adhesion promoters, and active metal and auxiliary metal are loaded through a pressurized stirring crystallization method, so that the specific surface area of the catalyst is effectively increased, and the specific surface area of the catalyst is increased. The dispersity of the loaded metal is improved, and the interaction between the metal and the Fe-Al2O3 carrier is enhanced. A methyl ethylbenzene dehydrogenation reaction result of the prepared catalyst shows that a target product can be prepared under the condition that the water-hydrocarbon ratio is as low as 0.8, and the catalyst is good in catalytic performance, high in stability, remarkable in technical and economic effects and beneficial to industrial popularization.

The invention discloses a synthesis method of a key intermediate of Tepotinib, which comprises the following steps: step (1), carrying out Suzuki coupling reaction on 3-methylphenylboronic acid and 2-iodo-5-bromopyrimidine to obtain a coupling product; step (2), carrying out Ullmann coupling reaction on the obtained coupling product and N-Boc piperidine-4-methanol under a strong alkaline condition; and step (3), converting N-Boc in a coupling product obtained by the Ullmann coupling reaction into N-methyl, and then carrying out benzyl bromination reaction to generate the key tepotinib intermediate. The synthesis method has the advantages of short steps, simple operation, mild reaction conditions, less by-products, high product purity and high product yield, and is suitable for large-scale production.