3218 results about "Chemical synthesis" patented technology

The invention relates to the field of preparation and application of biological peptides, in particular to a hippocampal swelling peptide and application thereof in preparation of functional products for repairing male reproductive system injury. A green controllable enzymolysis technology is utilized to obtain protein polypeptide with nutritional, health-care and medicinal values, five active peptide sequences with high biological activity are obtained through further research on the basis, the high-purity active peptide is obtained through a chemical synthesis mode, and the biological activity of the peptide is verified through mouse spermatogonium.

The invention relates to an inverse synthesis route planning method and system based on a multi-modal large model, and belongs to the technical field of chemical synthesis and artificial intelligence crossing. The method comprises the following specific steps: firstly, extracting three-dimensional molecular structure characteristics of a target product through a molecular encoder, and aligning the three-dimensional molecular structure characteristics with text modals of molecules; secondly, reasoning a possible reaction mechanism and a reaction type, and reducing an inverse synthesis search space; secondly, splitting a target product into reasonable synthesis subunits through structured marking and vocabulary expansion, data-driven atomic assignment learning and reaction center recognition and activity prediction; finally, SMILES representations and reaction paths of the reactants are generated. According to the method, the accuracy and interpretability of inverse synthesis path planning can be improved, and a new technical means is provided for automation and intellectualization in the fields of new drug development, material design and the like.

The invention relates to the field of microfluid chemical synthesis, and discloses a method for preparing gold nanoparticles based on two-phase flow microfluid control. The method comprises the following steps: 1) converging a gold precursor water phase, a reducing agent water phase and an organic phase in a micro-fluidic chip at 0-25 DEG C to form water-in-oil liquid drops; (2) conveying the fluid to a mixing area channel of a micro-fluidic chip, and carrying out instantaneous nucleation reaction to form a gold nanoparticle prototype; 3) conveying the fluid into a capillary reactor, and further nucleating, growing and curing the gold nanoparticle prototype; and (4) the fluid is subjected to phase splitting, and a gold nanoparticle solution is obtained. A three-in-one micro-fluidic chip is adopted, process parameters are optimized, and a gold precursor and a reducing agent are wrapped in an organic phase before reaction to form water-in-oil liquid drops, so that on one hand, the situation of adsorption and scaling of the inner wall of a channel can be avoided, and on the other hand, the heat and mass transfer efficiency of a material can be improved through the generated liquid drops; and the uniformity of a reaction nucleation environment is ensured.

The invention relates to the technical field of organic chemical synthesis, in particular to a preparation method of 3, 4 '-diaminodiphenyl ether.The preparation method comprises the steps that S1, under inert gas and in a first solvent, m-dinitrobenzene and p-acetamidophenol are subjected to a heating reaction under the condition of a weak base catalyst, and 3-nitro-4-acetamido diphenyl ether is prepared; s2, in a second solvent, the 3-nitro-4-acetamido diphenyl ether is subjected to a hydrogenation reduction reaction, and 3-amino-4-acetamido diphenyl ether is prepared; and S3, dissolving the 3-amino-4-acetaminodiphenyl ether in an alcohol solvent system, adding an aqueous solution of alkali, controlling the reaction temperature, carrying out a hydrolysis reaction, and after the reaction is finished, carrying out post-treatment to obtain the 3, 4 '-diaminodiphenyl ether. The preparation method provided by the invention has the advantages of easily available raw materials, low price, good selectivity and high product yield, and is more suitable for industrial production by comprehensively considering economical efficiency and safety.

The invention discloses a temperature measurement sensor data processing method and system in a chemical synthesis environment. The method comprises the steps of original data acquisition and preprocessing, sensor drift compensation, dynamic response optimization and anomaly detection and adaptive calibration. The system comprises an original data acquisition and preprocessing module, a sensor drift compensation module, a dynamic response optimization module and an anomaly detection and adaptive calibration module. Through multi-module deep fusion of LSTM drift compensation and adaptive Kalman filtering, + / -0.5 DEG C measurement precision is realized in a range of 80-300 DEG C; the MPC predictive control compresses the thermal inertia lag of the sensor from 500ms to less than or equal to 80ms, so that the sudden rising / dropping temperature in the synthesis reaction can be effectively captured, and the product decomposition caused by local overheating is avoided; isolated forest anomaly detection and least square calibration are combined, so that the maintenance period of the sensor in a strong corrosion environment is prolonged from 7 days to 90 days, and the annual maintenance cost is reduced by 65%.

The invention discloses an alcohol dehydrogenase mutant and application of the alcohol dehydrogenase mutant in asymmetric synthesis of (S)-6-hydroxy-8-chloro ethyl caprylate with optical purity. The alcohol dehydrogenase or the mutant thereof provided by the invention has extremely high conversion rate and can effectively improve the optical purity of the product. Moreover, based on the mutant, low-cost, efficient and rapid production of single-configuration ethyl 6-hydroxy-8-chloro caprylate can be realized, a multi-configuration mixture is not generated, and the problems of tedious steps, pollution and the like caused by a conventional chemical synthesis method are also avoided.

The invention discloses a preparation method and application of a chiral aldehyde amine condensation covalent organic framework material, through an ultrasonic chemical synthesis method, the synthesis cost and energy consumption are remarkably reduced, the reaction time is shortened, and the chiral transmission efficiency and the crystallinity of the material are greatly improved; the synthesis method disclosed by the invention not only has the characteristics of high efficiency and environmental protection, but also provides a brand new technical means for preparing a high-performance chiral two-dimensional COF material with a controllable structure; according to the preparation method, the preparation of the chiral two-dimensional COF material is more efficient and stable, and the chiral two-dimensional COF material has high repeatability and controllability, is suitable for being widely applied to various technical fields needing high-chiral materials, and further promotes the development of the chiral materials in scientific research and industrial application.

The invention relates to the technical field of chemical synthesis of dyes, in particular to a 5, 5 '-disubstituted amino-3, 3'-dipyridyl derivative as well as a preparation method and application of the 5, 5 '-disubstituted amino-3, 3'-dipyridyl derivative. According to the 5, 5 '-disubstituted amino-3, 3'-dipyridyl derivative and the preparation method thereof, the ornamental blue is used as a parent body for derivatization reaction, different structures are introduced to amino groups, the 5, 5 '-disubstituted amino-3, 3'-dipyridyl derivative is obtained and can be used as a dye, and the dye has relatively high color development intensity, bright color, deep dyeing and comprehensive color fastness. The preparation method of the 5, 5 '-disubstituted amino-3, 3'-dipyridyl derivative is continuous in process step, high in controllability, large in treatment capacity and suitable for large-scale industrial production, the 5, 5 '-disubstituted amino-3, 3'-dipyridyl derivative is applied to fabric dyeing, and the fabric has the advantages of washing resistance, acid resistance, sublimation resistance, wet friction resistance and the like.

The invention belongs to the technical field of medicines, cosmetics and scalp care, and particularly relates to application of coniferaldehydes and derivatives or salts of the coniferaldehydes to preparation of medicines and cosmetics for promoting hair regeneration and treating chemotherapy-induced alopecia (CIA, CIA) and other types of alopecia, in particular to application of the coniferaldehydes and the derivatives or salts of the coniferaldehydes to preparation of the medicines and the cosmetics. Experimental results show that coniferyl aldehyde can promote hair regeneration of mice, accelerate hair growth of the mice and effectively relieve alopecia symptoms of the mice after chemotherapy, and the effect of coniferyl aldehyde is better than that of minoxidil. According to the application, coniferyl aldehyde or a composition thereof is given to a subject, so that the vigor of hair follicles is remarkably enhanced, the stationary period of the hair follicles is shortened, and the hair loss process is inhibited. The coniferyl aldehyde provided by the invention has the industrial application advantages of reliable biological safety, controllable preparation cost and high raw material accessibility, can be obtained by a plant extraction or chemical synthesis method, is suitable for an external solution, gel or a scalp care preparation, and provides a natural, safe and effective solution for alopecia patients.

The invention discloses an antibacterial peptide based on D-type amino acid and application of the antibacterial peptide, and the antibacterial peptide is characterized in that the amino acid sequence is w-r-r-w-r-r-w-w-r-k-r (dTrp-dArg-dArg-dTrp-dArg-dArg-dTrp-dTrp-dArg-dLys-dArg). The antibacterial peptide can be synthesized through an Fmoc solid-phase chemical method, the synthesis difficulty is low, and the in-vivo antibacterial activity is good. The antibacterial peptide especially has broad-spectrum killing activity on carbapenem-resistant pseudomonas aeruginosa, pseudomonas aeruginosa, klebsiella pneumoniae, escherichia coli, methicillin-resistant staphylococcus aureus and staphylococcus aureus, is low in hemolytic toxicity, can reach half or more of cell survival rate under medium and low concentration, almost has no toxic effect on cells, and can be used for preparing the antibacterial peptide with a broad-spectrum killing activity on carbapenem-resistant pseudomonas aeruginosa, klebsiella pneumoniae, escherichia coli, methicillin-resistant staphylococcus aureus and staphylococcus aureus. The stability is good, the operability is high, and the cost is low.

The invention provides bacillus velezensis and application of the bacillus velezensis in co-production of 6-methyl-2-heptanone and 2, 4-di-tert-butylphenol, and belongs to the technical field of biological engineering. The bacillus velezensis is classified and named as bacillus velezensis LT-22, and is preserved in the China Center for Type Culture Collection (CCTCC), the preservation number is CCTCC NO: M2023779, and the preservation date is May 19, 2023. According to the bacillus velezensis, the 6-methyl-2-heptanone and the 2, 4-di-tert-butylphenol can be co-produced, and the concentrations of the synthesized 6-methyl-2-heptanone and the 2, 4-di-tert-butylphenol can reach 75.72 mg / L and 42.48 mg / L; compared with chemical synthesis, the method for preparing the 6-methyl-2-heptanone and the 2, 4-di-tert-butylphenol is low in production cost, simple to operate, high in safety, environment-friendly and suitable for industrial popularization.

The invention relates to the field of organic chemical synthesis, in particular to a synthetic method and application of pyrimidone compounds. The invention provides a synthesis method, reactants are o-amino heterocyclic formamide and triethyl orthoformate respectively, a solvent system is a hexafluoroisopropanol solvent, and a product is a heterocyclic pyrimidone compound. The reaction does not need strong acid or strong alkali conditions, does not need additional reducing agents or oxidizing agents, does not need transition metal catalysis, is economical and practical, the reaction conditions are relatively mild, and the synthesized pyrimidone compound has a good antibacterial effect.

The invention provides a beta '-sulfo-alpha, beta-unsaturated gamma-lactam derivative as well as a preparation method and application thereof, and belongs to the technical field of organic chemical synthesis. The beta '-thio-alpha, beta-unsaturated gamma-lactam derivative has a structure as shown in a formula I. According to the method disclosed by the invention, cesium carbonate is taken as alkali, and a molecular skeleton of the beta'-thio-alpha, beta-unsaturated gamma-lactam derivative is constructed through free radical coupling and olefin isomerization processes under the condition of blue light irradiation. Bioactivity evaluation shows that the beta '-sulfo-alpha, beta-unsaturated gamma-lactam derivative prepared by the method disclosed by the invention has an inhibition effect on MDA-MB-231 human breast cancer cells.

The invention provides a separation method of a catalyst for preparing butyraldehyde through propylene carbonylation, and relates to the technical field of chemical synthesis. The separation method comprises the following steps: carrying out flash evaporation separation and low-pressure evaporator evaporation on a material obtained by carrying out a propylene carbonylation reaction on propylene and synthesis gas as raw materials, obtaining a gas-phase material from a collecting tank of a low-pressure evaporator, and outputting a liquid-phase catalyst solution; the gas-phase material is subjected to condensation and gas-liquid separation, crude butyraldehyde is output, and obtained non-condensable gas returns to a liquid distribution chamber of the low-pressure evaporator; wherein the catalyst is acetylacetone triphenyl phosphorus silicification carbonyl rhodium, and the operation temperature of the low-pressure evaporator is 85-95 DEG C. By controlling the circulating air volume and the evaporation temperature, high-temperature deactivation of the catalyst is prevented, the service life of the catalyst is prolonged, and the process cost is reduced; the process flow is simplified, and the method is suitable for large-scale process production.

The invention relates to the technical field of environmental chemistry, in particular to a double-vacancy Fe0. 96S (at) MoS2 nano composite material as well as a wet-type mechanochemical synthesis method and application thereof. The preparation method comprises the following steps: firstly carrying out co-ball milling by utilizing a wet mechanical chemical synthesis method to obtain a low-crystallinity Fe0. 96S (at) MoS2 precursor, and then carrying out further calcination treatment to accelerate the thermal reaction of the precursor, improve the crystallinity and remove redundant sulfur powder impurities, thereby obtaining the high-crystallinity Fe0. 96S (at) MoS2 nano composite material. Iron powder is introduced in the process of preparing MoS2 nanosheets from molybdenum powder and sulfur powder, the reaction activity of the molybdenum powder and the sulfur powder is improved and the formation energy of MoS2 is reduced by utilizing the characteristic of ball-milling heat release of the iron powder and the sulfur powder, the reaction barrier that MoS2 is difficult to prepare between Mo and S through a mechanical ball-milling process originally is broken, and the generation of the MoS2 nanosheets is promoted.

The invention particularly relates to a saccharomyces cerevisiae genetically engineered bacterium for de novo synthesis of 7-DHC as well as a construction method and application of the saccharomyces cerevisiae genetically engineered bacterium and belongs to the technical field of biology. According to the invention, a saccharomyces cerevisiae engineering bacterium SC9 is taken as an original strain, multiple times of multiple copies of tHMG1, DHCR24 and ERG1 are carried out on TY transposon, multiple copies of ERG2, POS5, ERG7, ERG11, IDI1 and ERG3 are carried out on TY transposon, and POS5, ERG3 and DHCR24 are singly copied on a genome, so that the content of intracellular reducing coenzyme II is increased, and a main path for synthesizing 7-DHC is enhanced. The genome single copy ACL, ACS1, ERG10, ERG19 and the like are used for enhancing the utilization of saccharomyces cerevisiae ethanol and dynamically regulating and controlling the synthesis of 7-DHC. The saccharomyces cerevisiae gene engineering strain constructed by the invention has high product accumulation, and lays a foundation for replacing a traditional multi-step chemical synthesis route and realizing industrial production.

The invention discloses an antibacterial peptide fragment intercepted from chitinase IDGF4 protein and application of the antibacterial peptide fragment in preparation of antibacterial drugs. According to the invention, short peptide fragments in chitinase IDGF4 protein are screened, three candidate peptides are obtained through chemical synthesis, the antibacterial performance of the candidate peptides is systematically evaluated, and the evaluation result shows that the peptide fragment with the amino acid sequence as shown in SEQ ID No.2 can effectively inhibit the growth of salmonella and staphylococcus aureus under the concentration of 1mg / mL; the antibacterial effect of the compound is confirmed in inhibition zone experiments, enzyme-labeled turbidimetry and growth curve monitoring, and the compound shows stable and remarkable antibacterial activity and can be used as a novel antibacterial molecule; the invention provides a new candidate sequence for developing the antibacterial peptide with high efficiency and low drug resistance risk, and has application potential in the aspect of preparing clinical antibacterial drugs.

The invention relates to a textured KCu7S4 thermoelectric material and a preparation method thereof, and the method comprises the steps: sequentially adding a prepared KOH aqueous solution, CuCl2. 2H2O and Na2S. 9H2O into a high-pressure kettle, and fully stirring for dissolving; dropwise adding an N2H4.H2O aqueous solution into the mixed solution, fully stirring, sealing, transferring to a microwave chemical synthesis instrument, heating, keeping stirring, and reacting at a target temperature and self-generated pressure to generate a KCu7S4 nanowire preferentially growing along a [001] crystal orientation; and after the reaction is finished and natural cooling is carried out, a product is collected through centrifugation, full cleaning and vacuum drying are carried out, and then the KCu7S4 thermoelectric material with [001] preferred orientation in the direction perpendicular to the pressure direction is obtained through spark plasma sintering. According to the method, a surfactant and an organic solvent are not used, and macro, rapid, efficient and controllable preparation of the KCu7S4 nanowire is realized through a low-temperature, low-cost and low-energy-consumption microwave-assisted hydrothermal process.

The invention discloses a crown ether grafted polyarylether sulfone ion separation membrane as well as a preparation method and application thereof, and belongs to the technical field of ion separation membranes, collaborative optimization is realized through crown ether accurate grafting and ultrathin ordered membrane formation: a main chain of polyarylether sulfone is grafted with 4 '-aminobenzo-12-crown-4 to form an inherent channel adapted to Li, and the specific surface area of the main chain is increased; the ultrathin film is prepared by a water surface spreading method, and the ion transmission path is shortened. Finally, in a LiCl / MgCl system, Liion flux has high selectivity, high permeation-high selectivity cooperation is preliminarily realized, the chemical synthesis step can be amplified to a kilogram level, and after a DPAES-g-CE / dichloromethane solution is dropwise added to the water surface, the DPAES-g-CE / dichloromethane solution is rapidly spread to form a film without precise equipment; the raw materials are industrial-grade monomers and have no toxic residues, the membrane can be recycled and reused through dichloromethane, the equipment cost is reduced by about 90%, and industrialization is easy; the main chain of the polyaryl ether sulfone is high in rigidity and resistant to high temperature and chemical corrosion; crown ether grafting avoids molecular chain agglomeration, and the swelling rate is far lower than that of a traditional sulfonated membrane.

The invention discloses an omariglitazone intermediate as well as a synthesis method and application thereof, and belongs to the technical field of pharmaceutical chemistry synthesis. The invention provides a synthesis method of an omarigliflozin intermediate and application of the intermediate in synthesis of omarigliflozin. The key of the synthesis method provided by the invention lies in the deprotection process of polycyclic indole amide, nitrile groups are not hydrolyzed, indole carboxylic acid is generated with high selectivity, molecular lactamization is avoided in the condensation process with polycyclic imine B, and expensive amidation reagents such as HATU are not needed in the process, so that the synthesis method is simple and easy to implement. And the purpose of preparing omariglitazone with low cost and high yield is achieved. The synthesis method has the advantages of easily available raw materials, mild reaction conditions, small side reaction influence, simplicity and convenience in operation and high yield, improves the yield, is easy to purify, and is suitable for industrial production of omariglitazone.

The invention belongs to the technical field of chemical synthesis, and particularly relates to a preparation method of N, N '-bis (2-bromine / chloroethyl) diamino phosphonic acid (1-methyl-4-nitro-1H-imidazole-2-cyanogen) methyl ester, 4-methylimidazole is used as a raw material, and (1-methyl-4-nitro-1H-imidazole-2-cyanogen) methanol is synthesized through nitration, methyl substitution, bromine substitution, bromomethyl substitution, hydrolysis and substitution; the preparation method comprises the following steps: reacting phosphorus oxychloride with ethyl amine salt to synthesize N, N '-bis (2-bromoethyl) diamino phosphonic acid and N, N'-bis (2-chloroethyl) diamino phosphonic acid, and finally condensing to obtain N, N '-bis (2-bromoethyl) diamino phosphonic acid (1-methyl-4-nitro-1H-imidazole-2-cyanogen) methyl ester and N, N'-bis (2-chloroethyl) diamino phosphonic acid (1-methyl-4-nitro-1H-imidazole-2-cyanogen) methyl ester. The compound can selectively inhibit ovarian cancer cell proliferation under a hypoxia condition.

The invention discloses a preparation method for synthesizing coal-based carbon quantum dots through microbial catalysis, which comprises the following specific preparation steps: (1) pretreating coal, specifically comprising crushing and sterilizing treatment; (2) combining the pretreated coal sample with selected microorganisms or biological factors, and carrying out fermentation treatment on the coal; (3) after fermentation is completed, dialyzing the coal fermentation liquid to prepare a carbon quantum dot solution; (4) separating and purifying the dialyzed carbon quantum dot solution to remove impurities; and (5) carrying out quick freeze-drying on the separated and purified carbon quantum dot solution to obtain the carbon quantum dots with fluorescent properties. According to the method, microorganisms serve as a core, an aerobic or anaerobic fermentation process is combined, coal resources are fully utilized, and efficient preparation of the coal-based carbon quantum dots is achieved. The method not only has good environmental protection property, but also can provide a new technology for industrial production of the carbon quantum dots, and has important significance for efficient conversion and green chemical synthesis of coal.

The invention discloses an icaritin carbamate prodrug as well as a preparation method and application thereof, belongs to the field of pharmacy, and particularly relates to an icaritin carbamate prodrug as shown in a formula 3-N or 7-N and pharmaceutically acceptable salts thereof as well as a preparation method and application of the icaritin carbamate prodrug. Specifically, a main metabolic site (3-site or 7-site hydroxyl) of a natural flavone compound icaritin is subjected to structural modification through a chemical synthesis method, and an appropriate group is introduced into the site to form the icaritin carbamate prodrug. Amines adopted by the carbamate are aliphatic amines. Due to existence of a carbamate structure, II-phase metabolism of icaritin in SD rats is reduced, compared with icaritin raw material medicine, the 3-N-01 prodrug has the advantages that oral bioavailability is remarkably improved, the 3-N-01 prodrug is the optimal prodrug, clinical medication is expected to be capable of reducing administration dosage and improving patient compliance, and the 3-N-01 prodrug can be applied to preparation of the SD rats. And an effective strategy is expected to be provided for improving the oral bioavailability of phenolic drugs. # imgabs0 #

Disclosed herein are systems and embodiments for improving energy efficiency of a chemical separations plant through heat integration. Heat integration may provide heating loops between distillation columns and / or integrated electric heating components configured to supply heat to reboilers in the chemical separations plant. Heat integration may use heat from an associated chemical synthesis plant configured to carry out an exothermic reaction (e.g., production of methanol from CO2 and H2). Such integrated process designs allow for the use of “low-grade” heat, thereby improving energy efficiency. Furthermore, such integrated process designs allow for electrification of exemplary chemical separations plants, replacing the use of steam as a heating medium with more energy efficient and carbon-emission neutral, electrical methods.

The invention discloses a chiral alpha alkyl beta hydroxyl phosphate compound as well as a preparation method and application thereof, and belongs to the technical field of chemical synthesis. In the presence of a catalyst, carbonyl of a substrate is reduced into hydroxyl to obtain a chiral alcohol compound, alpha-alkyl beta-ketophosphonate is reduced by an asymmetric catalytic hydrogen transfer method, and a reduced product can be used as a core skeleton of various drug molecules, so that the chiral alcohol compound is prepared. The compound has an obvious promotion effect on migration and repair of keratinocytes, and has great application potential in the aspects of wound healing, skin tissue soothing, repair, aging resistance and the like.

The invention discloses a short peptide PRP1 as well as a preparation method and application thereof. Belongs to the technical field of gene engineering. According to the application, an oligopeptide which is derived from unknown protein and can regulate and control the resistance of tobacco to the potato Y virus disease is obtained through research and identification, the oligopeptide is named as PVY residual peptide (PRP1), the amino acid sequence of the oligopeptide is ATKHIVGSIVAS, the oligopeptide PRP1 is prepared through a chemical synthesis method, and the oligopeptide is injected into the tobacco at the seedling stage, so that the PVY virus quantity can be effectively reduced, and the resistance of the tobacco to the potato Y virus disease can be improved.

The invention discloses a high-oxidation-resistance long-life polyethylene cable sheath material and a preparation method thereof, and relates to the technical field of high polymer materials. Comprising the following components: high-molecular-weight high-density polyethylene, surface-modified nano-dioxide, furan-maleimide grafted polyethylene, a Schiff base dynamic cross-linking agent, tea polyphenol grafted polyethylene, a temperature-responsive oxygen-blocking microcapsule, a main antioxidant, an auxiliary antioxidant, an emergency antioxidant, a light stabilizer, a halogen-free flame retardant, a processing aid and an acid absorbent. According to the invention, the main antioxidant, the auxiliary antioxidant and the tea polyphenol grafted polyethylene form a chemically synthesized and naturally modified composite antioxidant system, the designed service life of the material is greatly prolonged, the temperature-responsive oxygen-blocking microcapsule automatically cracks to release the core material when the operating temperature of the cable is greater than or equal to 90 DEG C, a dynamic oxygen-blocking layer is formed, and the service life of the cable is prolonged. The defect that the effect of traditional physical oxygen barrier is attenuated at high temperature is overcome, and the oxygen permeability at high temperature is reduced compared with that of a single nano barrier scheme.

The invention relates to the technical field of chemical synthesis, and particularly discloses an alpha methyl beta phosphonate compound and a synthesis method thereof.The alpha methyl beta phosphonate compound is obtained by directly oxidizing the alpha position of aryl ketone into carbon positive and combining the carbon positive with diethyl phosphite anions under the alkaline condition by using hydrogen peroxide and iodine as oxidizing agents. The alpha methyl substituted beta phosphate ester compound can be generated by a one-step method. The method is suitable for synthesizing compounds of phosphoric acid (methyl, ethyl, propyl and the like) with different alkyl substitutes (methyl, ethyl, propyl and the like) at carbonyl alpha positions. According to the method, the alpha-methyl substituted beta phosphate compound can be synthesized only by using commercial cheap and easily available aryl ketone as a raw material, using hydrogen peroxide and iodine as oxidants and using diethyl hypophosphite as a phosphine source, and reacting in the DMSO solvent at 100 DEG C for 12 hours, so that the target product can be obtained, and the yield is excellent. Compared with previously reported methods, the method does not need low-temperature operation, is simple to operate, adopts a one-pot method, does not need a metal catalyst, and all raw materials are common bulk chemicals.

The invention provides a system and a method for co-production of synthesis gas with adjustable and controllable hydrogen-carbon ratio through carbonate reduction refining. The system comprises a hydrogen supply unit, a carbonate feeding unit and a carbonate fluidization hydrogenation reactor, the carbonate fluidization hydrogenation reactor comprises a first reaction chamber, a second reaction chamber and a cyclone separation unit; according to the system and the method for co-producing the synthesis gas with the adjustable hydrogen-carbon ratio through carbonate reduction refining, the reaction intensity of the first reaction cavity and the second reaction cavity of the carbonate fluidization hydrogenation reactor is adjusted and controlled, so that the hydrogen-carbon ratio in the product synthesis gas at the synthesis gas discharge hole can be accurately controlled; and proper reaction raw materials are directly provided for chemical synthesis of a series of subsequent high-added-value carbon derivatives.

The invention relates to a multi-robot chemical synthesis real-time scheduling control method based on MAS, and the method enables chemical synthesis resources to be mapped into intelligent agents with different functional attributes, and carries out the deep improvement through employing an MAS optimization scheduling mechanism. By carefully constructing an MAS real-time scheduling architecture model, optimizing a CNP negotiation mechanism and designing an efficient real-time scheduling method, efficient collaborative scheduling of diversified small-batch reaction tasks, multi-type robot workstations and multiple mobile robots is realized. Therefore, the overall efficiency and quality of chemical synthesis are remarkably improved, and the cost and the safety risk are reduced.