Abstract: [6,6]-Phenyl C71 butyric acid derivatives (C70-PCBR3) having a selectivity of greater than 95 wt % of the ?-isomer are provided by reacting fullerene C70 with a dialkyl sulfonium tetrafluoroborate having the formula:

Abstract: The present invention relates to a stripping method capable of recovering, by an environmentally friendly method, a high-purity ester-based compound without concern over the oxidation of an ester-based compound from a mixture containing the ester-based compound. The stripping method has advantages of generating no wastewater, enabling equipment costs to be reduced by simplifying the process, removing concern over the oxidation of an ester-based compound during the process, and enabling the reuse of the components recovered in the process.

Abstract: A reactive distillation method comprises introducing a feed stream to a reactive distillation column, wherein the feed stream comprises ethanol, contacting the feed stream with one or more catalysts in the reactive distillation column during a distillation, and removing butyl acetate during the distillation from the reactive distillation column as a bottoms stream. The feed stream reacts in the presence of the one or more catalysts to produce a reaction product comprising ethyl acetate, butanol, and water, wherein the butanol and the ethyl acetate react to produce a reaction product comprising the butyl acetate.

Abstract: A chemical reactor for use in a chemical process wherein a reactant and/or a target product is prone to produce undesirable byproducts through secondary reactions. The reactor is configured with a first flow passage for passing a flow of an overly reactive reactant; a permeable first wall for controlled flow of the overly reactive reactant into a second flow passage providing a flow of a second reactant; a permeable second wall having a catalyst supported on an inner surface thereof for catalyzing reaction of the reactants flowing in the second flow passage; the permeable second wall passing through a flow containing the target product; and a non-permeable third wall defining a third flow passage for exiting the product mixture. The reactor can be employed in selective oxidation, oxidative dehydrogenation, and alkylation processes to reduce the formation of byproducts.

Abstract: The purpose of the present invention is to provide: a ligand that is useful in a catalytic organic synthetic reaction; a method for producing said ligand; and a metal complex that is useful as a catalyst in an organic synthetic reaction. The present invention provides a compound represented by general formula (1A), a method for producing said compound, and a metal complex including said compound as a ligand. (In the formula, H, N, P, S, L, R1, R2, R3, Q1, and Q2 have the meaning as defined in the Description.

Abstract: Various embodiments disclosed relate to bridged phthalocyanine- and napththalocyanine-metal complex catalysts and methods of using and purifying the same. In various embodiments, the present invention provides a method of purifying a catalyst. The method includes contacting a catalyst composition with acid, the catalyst composition including a catalyst, to provide an acidified catalyst composition with the catalyst dissolved therein. The method includes precipitating the catalyst, and removing the precipitated catalyst from solution, to provide a purified catalyst.

Abstract: The present invention relates to a method for producing a hydride having a carbon number of 4, comprising contacting, in liquid phase, an unsaturated compound having a carbon number of 4 as a raw material with a solid catalyst obtained by loading a metal element belonging to Groups 9 to 11 of the long periodic table on a support, thereby performing hydrogenation to produce a corresponding hydride having a carbon number of 4, wherein hydrogenation is performed in the presence of, as a solvent, a 1,4-butanediol having a nitrogen component concentration of 1 ppm by weight to 1 wt % in terms of nitrogen atom.

Abstract: This invention is directed to methods of preparing AQX-1125 having the formula: This invention is also directed to intermediates utilized in the methods of preparing AQX-1125.

Abstract: By reacting 3-methyl-2-methoxymethylaniline, etc. with a phosgene compound in the presence of a tertiary amine at 10° C. to 14° C. in at least one kind of solvent selected from a group consisting of chlorobenzene and ortho-dichlorobenzene, an isocyanate compound such as 3-methyl-2-methoxymethyl-1-isocyanatobenzene can be manufactured with good yields.

Abstract: Carbon dioxide is reacted with methane in a free radical reaction to produce methanol and carbon monoxide. A system for producing carbon dioxide as a feed ingredient for the process through electric power generator is disclosed.

Abstract: Borylated compounds are disclosed, as well as their methods of preparation and their applications. The disclosed borylated compounds are highly stable, and have reduced band gap properties, thereby making them attractive candidates for incorporation into semiconducting materials for use in a variety of electronic, optical or electro-optical devices or components.

Abstract: The present invention also relates to a process for preparing a diamine/dicarboxylic acid salt wherein the dicarboxylic acid comprises an aromatic dicarboxylic acid and is provided in a powder form; the diamine is provided in a liquid form gradually dosed to the dicarboxylic acid powder, while keeping the dicarboxylic acid powder in constant movement; the processing temperature is above 0° C. and below the boiling temperature of the diamine and the melting temperature of the acid and the salt, and the reaction mixture comprises at most 5 wt. % of water. The present invention also relates to an anhydrous diamine/dicarboxylic acid salt obtainable by the process according to invention, or any embodiment thereof as described above.

Abstract: This invention relates to a method of continuously preparing acrylic acid and an apparatus using the same, the method including: (1) subjecting a feed including propane, oxygen, water vapor and carbon dioxide to partial oxidation using a catalyst, thus obtaining an acrylic acid-containing mixed gas, (2) separating the acrylic acid-containing mixed gas into an acrylic acid-containing solution and a gas byproduct, (3) separating an acrylic acid solution from the separated acrylic acid-containing solution, and (4) recycling the separated gas byproduct into the feed.

Abstract: The present invention relates to the manufacture of biobased acrylic acid from glycerol as starting material, the term “biobased acid” indicating that the acrylic acid is essentially based on a carbon source of natural origin.

Abstract: The principles of the present invention are useful in telomerization reactions in which ethylene and/or propylene taxogen is used in free radical reactions to make telomers of limited molecular weight, e.g., those in which a major portion of the telomer products are telomers incorporating 1 to 12 moles of ethylene and/or propylene per mole of telogen (i.e., a major portion of the telomer products incorporate telomers for which n is 1 to 12). The present invention is based at least in part upon the discovery that using a very large stoichiometric excess of C1 to C12 telogen(s) (i.e., telogens incorporating 1 to 12 carbon atoms per molecule) in combination with using very low concentrations of initiator provides telomerization reactions that are selective for producing lower molecular weight telomers.

Abstract: A method for producing a compound of formula (I) or a pharmaceutically acceptable salt, solvate, tautomer or stereoisomer, such as compound 1 and compound 2 is disclosed. The method proceeds through an O-allylated tyrosine-based compound, such as compound 3 and preferably comprises [3,3] sigmatropic Claisen rearrangement and olefin cross metathesis reactions. In addition, a pharmaceutical composition comprising a compound of formula (I) a tumor necrosis factor (TNF) related apoptosis inducing ligand (TRAIL) and a pharmaceutically acceptable carrier or excipient is disclosed.

Abstract: The invention relates to a method for producing alcohols by homogeneously catalyzed hydroformylation of olefins to aldehydes and subsequent hydration of the aldehydes. The invention further relates to a system for carrying out the method. The main focus is on the separation technique for work-up of the hydroformylation mixture. The problem addressed by the invention is that specifying a work-up method for hydroformylation mixtures that utilizes the specific advantages of known separation technologies but at the same time largely avoids the specific disadvantages of said separation technologies. The most important objective is to create a catalyst separation system that is as complete and at the same time conservative as possible and that operates in a technically reliable manner and entails low investment and operating costs. The method should be unrestrictedly suitable for processing the reaction output from oxo systems in “world scale” format.

Abstract: In an embodiment, a method of producing a bisphenol comprises reacting a phenolic compound with a reactant comprising one or both of an aldehyde and a ketone in the presence of a catalyst system and methanol to produce the bisphenol; wherein the methanol is present in an amount of 250 to 5,000 ppm based on the total weight of the reactant; wherein the catalyst system comprises an ion-exchange resin comprising a plurality of sulfonic acid sites; and 5 to 35 mol % of an attached promoter molecule based on the total moles of the sulfonic acid sites in the catalyst system; and wherein the attached promoter molecule comprises at least two thiol groups per attached promoter molecule.

Abstract: In a process for the production of higher alcohols, i.e. C4+ alcohols, from syngas, the syngas is first reacted in a heterogeneous alcohol pre-converter (A) using an alcohol synthesis catalyst, whereby methanol as the main product in a concentration corresponding to or close to the equilibrium concentration is produced. Then the effluent from the pre-converter is mixed with unconverted wet recycle gas and reacted in a heterogeneous reactor for higher alcohols synthesis (B) containing a higher alcohols synthesis catalyst, and finally the effluent from the reactor for higher alcohols synthesis is separated into (i) unconverted syngas, which is recycled to the higher alcohols synthesis reactor, (ii) methanol and light alcohols, which are recycled to the higher alcohols synthesis reactor, and (iii) the final product consisting of higher alcohols.

Abstract: The present invention provides an alkali metal salt of fluorosulfonyl imide having favorable heat resistance and a reduced content of specific impurities and a water content, and provides a method for producing an alkali metal salt of fluorosulfonyl imide, which is capable of easily removing a solvent from a reaction solution. An alkali metal salt of fluorosulfonyl imide of the present invention is represented by the following general formula (I) and has a mass loss rate of 2% or less when the alkali metal salt of fuluorosulufonyl imide is kept at 100° C. for 8 hours under an air current. A method for producing an alkali metal salt of fluorosulfonyl imide of the present invention comprises a step of concentrating a solution of the alkali metal salt of fulorosulfonyl imide by bubbling a gas into a reaction solution containing the alkali metal salt of fulorosulfonyl imide, and/or concentrating a solution of the alkali metal salt of fulorosulfonyl imide by thin layer distillation.