429 results about "Norbornene" patented technology

The invention discloses photocuring hydrogel capable of being combined with cytokines and used for tumor organoid culture and application, and belongs to the technical field of organoid culture. According to the invention, the hydrogel which can fix cells, can be combined with cell factors and can realize organoid recovery is developed through norbornene modified heparin, norbornene modified gelatin, sulfydryl four-arm polyethylene glycol, glucan, matrix metal protein peptidomimetic MMP and a photoinitiator. The hydrogel can be used for directly preparing organoids, heparin of various structures can be used, the cost is reduced, the modified heparin can bind factors or matrix protein and can controllably release the factors, the modified gelatin provides amino acid energy for collagen hydrolysate, and the hydrogel is formed by photocuring in a stepwise polymerization mode, is controllable in structure and can be used for preparing collagen collagen. The adjustable bionic modulus and the adjustable bionic stress relaxation are realized. The hydrogel disclosed by the invention can be used for culturing various organs, overcomes the problems of low repeatability, instability and the like in the prior art, and is suitable for the fields of tumor drug evaluation and the like.

The invention provides a novel polynorbornene anion exchange ionomer containing a polar functional group as well as a preparation method and application of the novel polynorbornene anion exchange ionomer. The polynorbornene has excellent thermal stability and chemical stability. Meanwhile, the AEI main chain of the polynorbornene has no aryl group, so that the adsorption influence caused by the aryl group is avoided. The synthesized addition polynorbornene AEI in the form of quaternary ammonium salt can be dissolved in a low-boiling-point solvent, and it is ensured that a membrane electrode can be prepared through a solvent casting method. Besides the solubility of the AEI, the addition polynorbornene-based AEI in the form of quaternary ammonium salt is modified by utilizing a thiol-ene click reaction, an anion exchange ionomer containing a polar functional group can be prepared, the interaction between the AEI and an electrolytic catalyst is improved, the reaction is simple and easy to operate, the universality is high, and the method is suitable for industrial production. And the current density in the AEMWE system containing the AEI can be effectively improved.

The invention discloses fast-curing modified polydicyclopentadiene resin as well as a preparation method and application thereof. The preparation method comprises the following steps: preparation of a polydicyclopentadiene resin system: dissolving a Grubbs second-generation catalyst and tributyl phosphite in cyclohexylbenzene to prepare a catalyst solution, and mixing the prepared catalyst solution with a dicyclopentadiene or norbornene-dicyclopentadiene mixed solution; preparing an epoxy resin system: adding an anhydride curing agent and an accelerant into epoxy resin and fully mixing; and mixing and stirring the epoxy resin system and the polydicyclopentadiene resin system, uniformly mixing, and storing at room temperature to obtain the modified polydicyclopentadiene resin. The curing degree of the modified PDCPD resin can reach 90-95% within 3-5 minutes under the condition of 60-90 DEG C. The modified PDCPD resin has good interface bonding with carbon fibers, glass fibers and basalt fibers, and the prepared composite material has excellent mechanical properties and high heat resistance.

The invention discloses a cycloolefin copolymer / carbon nanotube hybrid material modified oil-water separation sponge, relates to the field of high polymer materials, and provides a novel cycloolefin block copolymer which can be obtained by ring-opening metathesis polymerization of cycloolefin and 5-norbornene-2-carboxylic acid methyl ester under the catalysis of a third-generation Grubbs catalyst. The method is simple in process, and the length of the 5-norbornene-2-carboxylic acid methyl ester block can be accurately regulated, so that the nano shish-kebab structure and the surface performance of the nano shish-kebab structure can be regulated. The process for preparing the nano-hybrid shish-kebab from the cycloolefin block copolymer and the carbon nanotubes is simple in technology, the surface of a rough surface material such as polyurethane sponge can be uniformly covered with the nano-hybrid shish-kebab to form a thin film, super-hydrophobicity can be achieved, and meanwhile the nano-hybrid shish-kebab has oleophylic performance; and the oil-water separator has high separation efficiency and good wear resistance in the oil-water separation process.

The present invention relates to a matting agent for HAA powder coatings and a preparation method thereof. The matting agent is a matting polymer containing special groups such as hydroxyl and epoxy groups with significantly different activities. The matting polymer is mainly prepared from glycidyl methacrylate, methyl methacrylate, butyl acrylate, 5-norbornene-2-methanol, 2-methyl-3-butene-2-ol, dicyclopentadiene dioxide, a hydroxyl polyester resin, and an accelerator. Due to the presence of hydroxyl and epoxy groups of varying activities in its structure, supplemented by the accelerator and the physical dispersion effect during the preparation process, the product has excellent matting ability and good storage and matting stability. It can reduce the gloss of HAA system powder coatings to 3-10%.

A composition comprising decellularized extracellular matrices, hydrogels comprising the same, and methods of making the same are disclosed.

The invention relates to an aliphatic copolyester elastomer and a preparation method thereof, and belongs to the field of high polymer materials. The elastomer is prepared through a series ring-opening copolymerization reaction of epoxide and cyclic anhydride, and the method comprises the following steps: under the action of a metal-free catalyst (a phosphazene ligand P1-tert-octyl / triethyl boron system) and an initiator (terephthalyl alcohol), carrying out a series ring-opening copolymerization reaction on epoxide and cyclic anhydride, the preparation method comprises the following steps: reacting epoxide (such as epoxypropane and allyl glycidyl ether) with aliphatic anhydride (such as glutaric anhydride) in a xylene solvent to generate a polyester prepolymer retaining an active end; adding a second group of epoxide (such as cyclohexene oxide) and anhydride (such as tetrahydrophthalic anhydride and norbornene dianhydride), continuously reacting to form a block copolymer, and then crosslinking. The material performance can be regulated by changing the monomer combination, the atom economy is high, and the raw materials can be produced on a large scale. The process is simple and environment-friendly, and a new choice is provided for application of the degradable elastomer in the fields of medical treatment, environmental protection and the like.

The invention provides a barrier laser film and a preparation method thereof, the barrier laser film sequentially comprises a substrate layer, a barrier layer and a barrier adhesion layer from bottom to top, the barrier layer has a three-dimensional network structure and has hydrophobic styrene, norbornene and vinyl siloxane groups; the barrier adhesion layer is provided with a hydrophobic polyurethane chain segment, nano silicon dioxide particles and styrene, so that the hydrophobicity and the gas barrier property can be improved; both the barrier layer and the barrier adhesion layer have compact three-dimensional network structures and have reversible imine bonds generated by Schif alkali reaction of keto groups of diacetone acrylamide serving as a cross-linking agent and amino groups of primary amine, so that the density of the three-dimensional network structures can be further improved, and self-repairing of the three-dimensional network structures can be realized; the density of the three-dimensional network structure is maintained, and excellent gas barrier property and self-repairing property are realized through the synergistic effect of the two.

The invention discloses a carbon fiber modified sizing agent as well as a preparation method and application thereof. The preparation method of the carbon fiber modified sizing agent comprises the following steps: (1) reacting 5-norbornene-2-methylamine with monofunctional epoxy resin to obtain slurry; and (2) dissolving the slurry prepared in the step (1) in an organic solvent to prepare the modified sizing agent. And then obtaining the modified carbon fiber through a dipping and sizing process. The method is simple in process, and the interface bonding strength of the carbon fibers and the polydicyclopentadiene can be greatly improved.

The invention provides a preparation method of a multi-layer co-extrusion composite insulating material, and relates to the technical field of battery material manufacturing. The preparation method comprises the following steps: respectively melting and mixing an upper layer component, a middle layer component and a lower layer component which are respectively prepared, co-extruding, casting and forming to obtain a multi-layer membrane; performing two-way stretching on the multiple layers of membranes to obtain a composite insulating material; wherein raw materials adopted by the middle layer component comprise isotactic polypropylene and graphene in-situ polymerized polystyrene, raw materials adopted by the upper layer component comprise isotactic polypropylene and norbornene dianhydride, and raw materials adopted by the lower layer component comprise isotactic polypropylene and norbornene dianhydride. According to the obtained composite insulating material, good bonding strength exists between the layers and between the composite insulating material and the metal layer, and the composite insulating material is especially suitable for being used as a base film of a composite current collector.

The invention discloses polyolefin artificial leather, a preparation method thereof and an automobile seat, and belongs to the technical field of polyolefin artificial leather. The polyolefin artificial leather comprises a base cloth layer, a high-elasticity and high-softness layer and a coating layer which are sequentially stacked, the high-elasticity and high-softness layer comprises the following raw material components: a polyolefin elastomer, a low-density polyolefin elastomer, modified high-elasticity resin, an assistant crosslinker, a coupling agent and an anti-aging agent; the low-density polyolefin elastomer comprises a modified polyolefin elastomer, inorganic microspheres and a silane coupling agent; the modified polyolefin elastomer is prepared by grafting 4-vinyl-1, 2-phthalic acid and maleic anhydride on a polyolefin elastomer by adopting a melt grafting method; the modified high-elasticity resin comprises a high-elasticity polyolefin elastomer, a rubber elastomer, a silane coupling agent and a peroxide cross-linking agent; the high-elasticity polyolefin elastomer is obtained by copolymerization of propylene, norbornene and cardanol; p-chlorophenyl trimethoxy silane is at least adopted as the coupling agent.

The invention provides antibacterial silk fibroin hydrogel as well as a preparation method and application thereof, and relates to the technical field of biomedical materials. The antibacterial silk fibroin hydrogel provided by the invention is prepared from the following components: modified silk fibroin and copper montmorillonite, the modified silk fibroin is at least one of glycidyl methacrylate modified silk fibroin, methacrylic anhydride modified silk fibroin, isocyanate ethyl methacrylate modified silk fibroin and norbornene anhydride modified silk fibroin, and chemical crosslinking is formed among molecules of the modified silk fibroin. The copper montmorillonite and the modified silk fibroin form physical crosslinking through hydrogen bonds, and the mass ratio of the modified silk fibroin to the copper montmorillonite is 100: (1-10). The antibacterial silk fibroin hydrogel provided by the invention has good biological safety, long-acting antibacterial property, electrical conductivity and good mechanical property.

To obtain a copolymer which has a high crosslinking rate and excellent productivity and can form a molded product with thermal aging resistance, small compression set at high and low temperatures, and improved low-temperature characteristics (low-temperature elastic recovery characteristics and Gehman torsion characteristics), a composition containing the copolymer, and the like.SOLUTION: An ethylene / α-olefin / nonconjugated polyene copolymer (A) has a structural unit derived from ethylene [A1], a structural unit derived from a C4-20 α-olefin [A2], and a structural unit derived from a nonconjugated polyene [A3] having two or more partial structures selected from the group consisting of the following general formulae (I) and (II) in total in one molecule and satisfies specific requirements. The structural unit derived from the [A2] contains a structural unit derived from 1-butene, and the structural unit derived from the [A3] contains a structural unit derived from 5-vinyl-2-norbornene.SELECTED DRAWING: None

The invention discloses a cycloolefin block copolymer oil-water separation film, relates to the field of high polymer materials, and provides a method for preparing a cycloolefin block copolymer through ring-opening metathesis polymerization of cycloolefin and 5-norbornene-2-carboxylic acid methyl ester under the catalysis of a third-generation Grubbs catalyst. And the hybrid shish-kebab is prepared by using the polymer, so that an oleophylic and hydrophobic film structure can be formed, the prepared film can be effectively hydrophobic and has oleophylic performance, and a new treatment mode is provided for sewage prevention and treatment. The whole preparation process is simple in technology, rapid and batch production can be achieved, and popularization is convenient.

The invention relates to the technical field of cables, in particular to a multi-layer co-extrusion cable based on a low-smoke halogen-free flame-retardant composite layer and a preparation method of the multi-layer co-extrusion cable based on the low-smoke halogen-free flame-retardant composite layer, and the multi-layer co-extrusion cable structurally comprises a conductor layer, a double-layer insulating layer, a reinforced buffer layer and a composite sheath layer from inside to outside in sequence; wherein the double-layer insulating layer comprises an inner layer and an outer layer; the inner layer takes an ethylene-octylene copolymer as a core layer and takes a norbornene dianhydride grafted polyether ester elastomer as a shell layer, so that the material is endowed with high elasticity and impact resistance, and the cracking of the insulating layer is inhibited; the modified nano montmorillonite is dispersed into a nano lamellar barrier, so that heat diffusion is delayed, and low smoke and zero halogen are realized; the outer layer is composed of an ethylene-methyl acrylate matrix and di-tert-butyl phosphinic acid aluminum salt, the di-tert-butyl phosphinic acid aluminum salt is decomposed at high temperature to generate aluminum phosphate, a carbon layer is formed to isolate oxygen heat, and phosphorus-containing free radicals capture active free radicals to interrupt flame propagation.

The invention belongs to the field of biomedical engineering and medical materials, and discloses a hydrogel combined reagent, tough hydrogel can be prepared based on the hydrogel combined reagent, the tough hydrogel is based on brand-new dual-network hydrogel, the network of the tough hydrogel is composed of a PEGMA / GelNB covalent cross-linked network and a PEGMA self-cross-linked network, norbornene serves as a rigid structure, and the hydrogel combined reagent can be used for preparing the tough hydrogel. The hydrogel composition reagent has the advantages that the hydrogel composition reagent has a spring-like effect in a gel network, the stretching and compression performance of the hydrogel can be remarkably improved, and the tough hydrogel prepared from the hydrogel composition reagent has good biological activity and excellent mechanical property and can be quickly gelatinized under mild conditions.

The invention discloses a high-temperature-resistant poly (4-methyl-1-pentene) dielectric film with synergistically improved insulating strength and dielectric property and a preparation method and application thereof, and belongs to the field of preparation processes of polymer energy storage dielectric materials. The invention aims to solve the problems that the existing polymer energy storage material is low in energy storage density at high temperature, and the dielectric property and the insulating strength cannot be improved at the same time. The invention provides a method for preparing a norbornene dianhydride grafted poly (4-methyl-1-pentene) film by a two-step method by using poly (4-methyl-1-pentene) particles, norbornene dianhydride and dicumyl peroxide and combining a solution suspension technology with a melt casting extrusion technology and a one-way stretching traction technology. The high-temperature-resistant poly (4-methyl-1-pentene)-based dielectric film prepared by the invention has excellent breakdown strength and dielectric property, and the discharge energy density is as high as 5.92 J / cm < 3 > when the charge-discharge efficiency is greater than or equal to 90% at 150 DEG C.

The invention provides a method for preparing tetracyclododecene in a reactive distillation device by taking C9 fraction and norbornene as raw materials. The method comprises the following steps: mixing the C9 fraction and the norbornene in a mixer and reacting in the reactive distillation device; the reacted material is directly rectified in a reaction rectification device, residual C9 fraction and norbornene in the reaction are obtained at the tower top, and a crude tetracyclododecene product is obtained in the reaction kettle; and separating high-boiling-point components from the crude tetracyclododecene product in the reaction kettle section of the rectifying tower in the reactive distillation device in a third rectifying tower to obtain the high-purity tetracyclododecene product. According to the invention, the reaction rectification device is used, and the reactor is combined with the rectification tower, so that the reaction product can be directly and preliminarily separated to obtain a light component mainly containing norbornene and a heavy component containing tetracyclododecene, the equipment cost can be saved, the energy consumption can be reduced, and the rectification effect can be improved; meanwhile, the C9 fraction is used as a raw material, and downstream application of the C9 fraction is expanded.

The invention discloses a polymer based on side-chain liquid crystal polynorbornene as well as a preparation method and application thereof, a monomer based on side-chain liquid crystal polynorbornene has a structure as shown in a general formula 1, and the polymer based on side-chain liquid crystal polynorbornene has a repeating unit as shown in a general formula 8. According to the monomer structure, a benzamide group is introduced into a side chain liquid crystal molecular structure, adjacent liquid crystal side chains generate hydrogen bond interaction after polymerization, on one hand, the mechanical property of the material is improved, on the other hand, stacking arrangement of a layered structure can be promoted during film preparation, and the gas barrier performance is improved.

The invention belongs to the field of high polymer materials, and particularly relates to a cycloolefin polymer as well as a preparation method and application thereof. The preparation method provided by the invention comprises the following steps: a) in the presence of a catalyst system, carrying out prepolymerization reaction on a polymeric monomer in a solvent to obtain a prepolymer; the polymeric monomer comprises norbornene cycloolefin, and the viscosity of the prepolymer at 25 DEG C is 3-300 cps; and b) continuously mixing the prepolymer with a polymerization monomer for polymerization reaction, and then carrying out hydrogenation reaction on a polymerization reaction product to obtain the cycloolefin polymer. The cycloolefin polymer with excellent tensile strength, tensile modulus and film thickness uniformity can be obtained by adopting a two-step method for polymerization and controlling the viscosity of the prepolymer.

The invention relates to the technical field of electronic materials, in particular to a copper-clad plate resin composition with an ultralow-loss medium and a preparation method of the copper-clad plate resin composition. The composition comprises the following components: modified polyphenyl ether, dicyclopentadiene epoxy resin, trifunctional epoxy resin, active ester, cyanate ester, DMAP, spherical silicon dioxide and a POSS-silicon dioxide compound, the preparation method comprises the following steps: carrying out surface norbornenylation modification on bimodal spherical silicon dioxide, and carrying out click reaction on the bimodal spherical silicon dioxide and octa-aminophenyl polysilsesquioxane with tetrazinyl at the tail end to prepare a POSS-silicon dioxide compound, so as to construct an interface transition layer with gradient modulus. According to the invention, collaborative optimization of dielectric loss, thermal mechanical properties and interface bonding strength is realized, and the material has excellent properties of low dielectric loss, high thermal stability, high peel strength and the like, and is suitable for the fields of 5G communication, high-frequency electronic equipment and the like.

The invention discloses a low-residue lithium battery positive electrode tab film adhesive material and a preparation method thereof, and belongs to the technical field of lithium battery auxiliary materials. The preparation method comprises the steps of copolymer synthesis, premixing, filler dispersion, crosslinking system introduction and defoaming, and coating and packaging, the copolymer is prepared by norbornene, hexafluorobutyl acrylate and maleic anhydride free radical copolymerization, and fluorinated hyperbranched polyester is subjected to ester exchange and epoxy ring opening one-step functionalization. Aiming at the problems of high high-temperature residue, weak interface adhesion and poor electrolyte resistance of the existing adhesive, the invention designs that a fluorine-containing copolymer with high thermal stability and high reaction activity is taken as a main body and is matched with a reactive compatibilizer to construct a strong chemical bonding interface, and a hyperbranched stabilizer with double functions of physical binding and chemical chelation is introduced, so that the adhesive is prepared. The tab adhesive film bonding material with ultralow residue, ultrahigh peel strength and excellent electrolyte resistance is successfully prepared, and the long-term reliable sealing requirement of a high-energy-density lithium battery can be met.

The application belongs to the technical field of organic compound synthesis and the field of polymer preparation, and discloses a method for directly preparing a cycloolefin copolymer from dicyclopentadiene and ethylene based on a continuous flow reactor; the continuous flow reactor is used to efficiently prepare norbornene and derivatives thereof from ethylene and dicyclopentadiene, and then the norbornene and derivatives thereof are used to prepare a cycloolefin copolymer from excessive ethylene. The application uses dicyclopentadiene and ethylene as raw materials, realizes a continuous process from the synthesis of a cycloolefin monomer to the preparation of a cycloolefin copolymer, and the cycloolefin monomer does not need to be separated and stored and can directly participate in the polymerization reaction, so that the original complicated process is effectively simplified, energy consumption is reduced, the catalyst in the polymerization stage is not easy to be deactivated even at high temperature, the catalytic efficiency is high, and a high polymer yield can be obtained in a very short time.

The invention discloses a preparation method of an anti-pollution modified polyethersulfone nanofiltration membrane, which comprises the following steps: step A1, preparation of a membrane casting solution and a coagulating bath: dissolving polyethersulfone, a zwitterionic block copolymer, tetrazine modified graphene quantum dots and tetrabutyl titanate in N-methyl pyrrolidone to obtain the membrane casting solution; the zwitterionic block copolymer forms a dynamic hydration layer through strong hydration to inhibit pollutant adsorption; dissolving calcium chloride and disodium hydrogen phosphate in deionized water, adding triethanolamine to adjust the pH value of the solution to 8.0-9.0, continuously stirring, and adding norbornene modified chitosan in the stirring process to obtain a coagulating bath; the invention relates to the technical field of nanofiltration membranes. According to the preparation method of the anti-pollution modified polyethersulfone nanofiltration membrane, vertical array hydroxyapatite whiskers generated by biomimetic mineralization provide a super-hydrophilic surface to reduce organic matter adhesion; the tetrazine-norbornene light-triggered dynamic cross-linked network endows the film surface with self-repairing capability, and the use damage can be repaired.

The present application relates to bicyclo[2.2.1]hept-5-en-2-ol and related compounds, methods of making them, and methods of using them as flavor and fragrance ingredients in food, cosmetic, pharmaceutical, consumer, and other compositions and products.

The invention discloses a tetracyclododecene preparation method, which comprises: mixing an N-methyl pyrrolidone (NMP) solvent, norbornene and toluene, heating to a reaction temperature in a reaction kettle, dropwise adding cyclopentadiene, and carrying out a Diels-Alder reaction in the reaction kettle to prepare tetracyclododecene, the high-purity tetracyclododecene with the mass content of 99% or above can be obtained through subsequent rectification. According to the process, cyclopentadiene is dropwise added, so that the reaction time is shortened, side reactions are reduced, the reaction is carried out in a liquid phase by taking NMP (N-Methyl Pyrrolidone) with a higher boiling point as a solvent, the reaction temperature can be reduced, the reaction process can be carried out at normal pressure, the production safety is improved, and the production operation cost is reduced.

The invention discloses benzo [4, 5] imidazo [2, 1-a] isoquinoline compounds as well as a preparation method and application thereof, and belongs to the technical field of biological medicines. The benzo [4, 5] imidazo [2, 1-a] isoquinoline compound can be used for preparing anti-tumor (human breast cancer) drugs, the structure of the benzo [4, 5] imidazo [2, 1-a] isoquinoline compound is shown in the specification, in the formula, R1 is any one or two of hydrogen, halogen, alkyl, alkoxy, fused ring and aryl; r2 is any one of hydrogen, halogen, alkyl and alkoxy; and R3 is any one or two of hydrogen, halogen, alkyl and alkoxy. The preparation method of the compound comprises the following steps: by taking palladium acetate and norbornene as catalysts, tris (4-chlorphenyl) phosphine and the like as ligands, potassium carbonate and the like as alkali and 1, 4-dioxane as a solvent, carrying out one-pot synthesis on a 1-(2-bromo-1-phenyl vinyl) benzimidazole compound and an iodobenzene compound in an argon atmosphere. Structure of compound: # imgabs0 #

The invention discloses a preparation method of N-hydroxyl-5-norbornene-2, 3-dicarboximide sulfonate, which is characterized in that the N-hydroxyl-5-norbornene-2, 3-dicarboximide sulfonate is used as a raw material. The preparation method comprises the following step: in the presence of alkali, carrying out esterification reaction on a compound II and a compound III in a solvent to obtain a compound I. The preparation method disclosed by the invention can be used for obtaining a high-purity product with high yield and has a good industrial production prospect.

The invention discloses a paper-plastic composite reactive polyurethane hot melt adhesive for low-temperature coating, and belongs to the technical field of polyurethane adhesives, the paper-plastic composite reactive polyurethane hot melt adhesive for low-temperature coating comprises the following components by weight: 50-70 parts of modified polyester polyol, 30-50 parts of modified polyether polyol, 15-24 parts of diisocyanate, and 5-30 parts of tackifying resin, 0.1-1 part of a catalyst, 5-35 parts of a filler, 0.05-2 parts of a polymerization inhibitor and 0.1-0.5 part of an antioxidant; the modified polyester polyol is modified poly (butylene succinate); the modified polyether polyol is modified polypropylene glycol; the polyurethane hot melt adhesive prepared by modifying 5-norbornene-2-methylamine with a strong polar bond-NH and 3, 7-dimethyl octyl-6-ene-1-alcohol containing an insect-proof and mildew-proof functional component with polyhydric alcohol has relatively low melting temperature and viscosity, has initial viscous force of more than 1N and final viscous force of more than 5N at the same time, and has the characteristics of high temperature resistance, high temperature resistance, high temperature resistance and the like. The method can be well applied to paper-plastic compounding for low-temperature coating.

The invention discloses a synthesis method of 9-dichloromethylene-5-amino-benzonorbornene and an intermediate product, the synthesis method comprises the following steps: firstly, synthesizing a cyclization compound 1 as shown in a formula 1 from a cold solution of 6, 6-dichlorofulvene and 1, 4-benzoquinone under the action of a solution of a catalyst I, carrying out oximation reaction on the cyclization compound 1 prepared in the step a and hydroxylamine salt under an alkaline condition, and carrying out post-treatment to obtain the 9-dichloromethylene-5-amino-benzonorbornene. Under the action of a catalyst II, adding the oximate 2 prepared in the step b into a closed container, carrying out hydrogenation reduction to obtain 9-dichloromethylene-5-amino-benzo norbornene, and directly treating the reduction product with acid to obtain 9-dichloromethylene-5-amino-benzo norbornene, namely the 9-dichloromethylene-5-amino-benzo norbornene, namely the 9-dichloromethylene-5-amino-benzo norbornene. According to the method, the cyclization compound is oximated firstly, then the residual carbonyl and two double bonds on the ring are subjected to one-step reduction through catalytic hydrogenation, the working procedure is optimized, meanwhile, reduction by using expensive sodium borohydride is avoided, the method is short in synthesis route and suitable for industrialization, and the production cost is reduced.