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9 results about "Pentene" patented technology

Pentenes are alkenes with chemical formula C₅H₁₀. Each contains one double bond within its molecular structure. There are a total of six different compounds in this class, differing from each other by whether the carbon atoms are attached linearly or in a branched structure, and whether the double bond has a cis or trans form.

Layered nanosheet ferrierite molecular sieve as well as preparation method and application thereof

InactiveCN108793189AThe synthesis method is simpleMild conditions for crystallizationMaterial nanotechnologyHydrocarbon by isomerisationChemistryLow-density polyethylene
The invention discloses a layered nanosheet ferrierite molecular sieve. The nanosheet ferrierite molecular sieve is characterized in that the molecular sieve is a high-crystallinity pure-phase ferrierite molecular sieve; the thickness of the sheet is between 30nm to 80nm; the specific surface area is larger than or equal to 340m<2> / g; the mesoporous surface area is larger than or equal to 60 m<2> / g; the crystallinity reaches 109% or more and is larger than or equal to 106%. The invention also relates to a preparation method of the layered nanosheet ferrierite molecular sieve and application ofthe layered nanosheet ferrierite molecular sieve to alkene oligomerization, low-density polyethylene cracking and skeleton isomerization reaction in n-butene and n-pentene.
Owner:CHINA UNIV OF PETROLEUM (BEIJING)

Process for preparing 2-amylene by separating C5 distillate of petroleum

ActiveCN101289361ADistillation purification/separationPetroleumPentene
The invention discloses a method which is used for preparing 2-pentene by separating petroleum C5 fraction and takes raffinate C5 obtained after separating diolefin and isoamylene by extracting as raw materials. The process comprises that the raw materials are extracted and distilled, and the extractant is N and N-dimethylformamide, and the feeding weight ratio of the raw materials and the extractant is 1:5 to 1:12, C5 saturated hydrocarbon materials are discharged from a column top and the materials richly containing 2-pentene and the extractant are obtained in a column bottom; the materials in the column bottom obtained in the process 1 are distilled so as to recycle the extractant, and the materials richly containing 2-pentene are obtained in the column top, and the extractant is obtained in the column bottom, and the extractant can be recycled; the materials in the column top obtained in the process 2 are distilled and separated so as to remove light components, and the materials with light components are discharged from the column top, and the crude product of 2-pentene is obtained in the column bottom; and the crude product of 2-pentene obtained in the process 3 is distilled and refined so as to remove heavy components, materials in the column top are taken and a refined product of 2-pentene is obtained. By processing at a much deeper degree, the method of the invention solves a technical problem that 2-pentene in C5 fraction can not be utilized by the prior art.
Owner:SINOPEC SHANGHAI PETROCHEMICAL CO LTD +1

Solid acid catalyst for synthesizing 2-propyl-1,3-dioxocyclo-5-pentene and preparation method thereof and method for using solid acid catalyst to synthesize 2-propyl-1,3-dioxocyclo-5-pentene

The invention discloses a solid acid catalyst for synthesizing 2-propyl-1,3-dioxocyclo-5-pentene. A sulfonic acid group is grafted on the surface of a carrier silicon dioxide, and the preparation method of the solid acid catalyst comprises the steps that an organosilicone coupling agent containing a mercapto group is grafted to a carrier material loading silicon dioxide by adopting a post graftingmethod, and then the solid acid catalyst is prepared through the processes of oxidation, acidification and the like. The method for using the solid acid catalyst to synthesize the 2-propyl-1,3-dioxocyclo-5-pentene comprises the steps that the solid acid catalyst reacts with 1, 4-butylene glycol, n-butanal and a water-carrying agent, heating is conducted till no water is generated in the water diversion backflowing process, filtering and reduced pressure distillation are conducted, cut fraction under the vacuum degree of -0.098MPa and at the boiling point of 100-120 DEG C is collected, and theproduct 2-propyl-1,3-dioxocyclo-5-pentene is obtained. The provided solid acid catalyst has the advantage that equipment is not corroded, no waste water is drained out, the cost is low, the yield ishigh, and the catalyst is liable to being recycled and used repeatedly.
Owner:ZHEJIANG OCEAN UNIV

Preparation method of pyroxsulam intermediate

ActiveCN113292487AAvoid Polymerization Side ReactionsGuaranteed purityOrganic compound preparationCarboxylic acid esters preparationAcyl groupDouble bond
The invention discloses a preparation method of a pyroxsulam intermediate, which comprises the following steps: (1) carrying out condensation reaction on 4-alkoxy-1,1,1-trifluoro-3-buten-2-one and phosphonoacetic acid trialkyl ester in an alcohol solvent in the presence of sodium alcoholate to generate an intermediate 3-trifluoromethyl-5,5-dialkoxy pentenoic acid alkyl ester and an isomer of the intermediate 3-trifluoromethyl-5,5-dialkoxy pentenoic acid alkyl ester; and (2) carrying out cyclization reaction on the intermediate generated in the step (1) and ammonium acetate in the presence of a polymerization inhibition catalyst to generate 2-hydroxy-4-trifluoromethylpyridine. According to the method disclosed by the invention, hydroquinone and other polymerization inhibition catalysts are added in the cyclization process, so that polymerization side reaction of a condensation intermediate containing double bonds can be avoided, and the reaction yield and the product purity of the cyclization reaction are ensured. Meanwhile, the 4-butoxy-1,1,1-trifluoro-3-buten-2-one and the phosphonoacetic acid trimethyl ester are adopted as the condensation reaction raw materials, so that not only can higher condensation reaction yield be obtained, but also the cost is lower, and the safety is higher.
Owner:JIANGSU AGROCHEM LAB CO LTD
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