| Class / Patent application number | Description | Number of patent applications / Date published |
|---|
| 568343000 | Aldehyde or ketone reactant | 19 |
| 20090264681 | Process for Synthesis of (3R,3'R,6'R)-Lutein and its Stereoisomers - (3R,3′R,6′R)-Lutein and (3R,3′R)-zeaxanthin are two dietary carotenoids that are present in most fruits and vegetables commonly consumed in the US. These carotenoids accumulate in the human plasma, major organs, and ocular tissues. In the past decade, numerous epidemiological and experimental studies have shown that lutein and zeaxanthin play an important role in the prevention of age-related macular degeneration (AMD) that is the leading cause of blindness in the U.S. and Western World. The invention provides a process for the synthesis of (3R,3′R,6′R)-lutein and its stereoisomers from commercially available (rac)-α-ionone by a C | 10-22-2009 |
| 20100041922 | METHOD FOR THE ENANTIOSELECTIVE PRODUCTION OF OPTICALLY ACTIVE 4-HYDROXY-2,6,6-TRIMETHYL-CYCLOHEX-2-ENONE DERIVATIVES - The present invention relates to a process for enantioselectively preparing optically active 4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-one derivatives of the formulae (I) or (Ia) and to a process for preparing (3S,3′S)-astaxanthin of the formula (III), comprising the process for preparing the compound of the formula (I). | 02-18-2010 |
| 20110218364 | Synthesis and Use of Intermetallic Iron Palladium Nanoparticle Compositions - An intermetallic magnetic compound of iron oxide and palladium with a nanometer particle size is disclosed, together with a method of making magnetic nanoparticles that include an intermetallic bond between palladium and iron-oxide. Additionally, a method is disclosed of catalyzing an organic reaction by contacting the organic reagents with an intermetallic magnetic compound of iron oxide and palladium that has nanometer particle size in an amount sufficient to catalyze the organic reaction. | 09-08-2011 |
| 20120316365 | Dehydrogenation Process - In a process for the dehydrogenation of cyclohexanone to produce phenol, a feed comprising cyclohexanone is contacted with a catalyst comprising an inorganic, crystalline, mesoporous support material and a hydrogenation-dehydrogenation component under dehydrogenation conditions effective to convert at least part of the cyclohexanone in the feed into phenol and hydrogen. | 12-13-2012 |
| 568344000 | Oxidation utilizing gaseous oxygen | 1 |
| 20130172625 | METHODS FOR USING ALLYLIC OXIDATION CATALYSTS TO PERFORM OXIDATION REACTIONS - Methods for using ailylic oxidation catalysts to perform oxidation reactions. In an exemplary method for catalyzing an ailylic oxidation reaction of the present disclosure, the method comprises the step of catalyzing an oxidation of an ailylic compound using an ailylic oxidation catalyst. In at least one embodiment, the ailylic oxidation catalyst comprises palladium, gold, and titanium, In an exemplary embodiment, the ailylic oxidation catalyst comprises 2.5% Aυ÷2.5% Pd/TiO | 07-04-2013 |
| 568345000 | Aldehyde reacted with ketone | 3 |
| 20080234521 | CRYSTAL FORMS OF ASTAXANTHIN - Mixtures of specific crystal forms of astaxanthin and the individual crystal forms designated crystal Form I and II and disclosed together with methods for preparing said crystal Forms. Methods for preparing nutritional dosage forms including the disclosed astaxanthin crystal forms for the life science industry are also disclosed. | 09-25-2008 |
| 20100063325 | NOVEL PROCESS FOR THE PREPARATION OF TIMBERONE - This invention relates to a novel process for the preparation of timberone useful for perfume or cosmetics. | 03-11-2010 |
| 20110009673 | PROCESS FOR PRODUCING 2-(1-HYDROXYALKYL)CYCLOALKANONE - The present invention relates to a process for producing a 2-(1-hydroxyalkyl)cycloalkanone which includes the steps of (i) continuously mixing a cycloalkanone and an alkyl aldehyde in the water and a base catalyst to form a reaction system and allow both the compounds to react with each other; (ii) continuously withdrawing a reaction mixture produced in the step (i) out of the reaction system while allowing the step (i) to proceed; and (iii) adding an additional amount of water containing the base catalyst to the reaction system to maintain a constant concentration of the base catalyst and/or a constant amount of water in the reaction system while allowing the step (ii) to proceed. | 01-13-2011 |
| 568346000 | Reactant contains -COO- group | 1 |
| 20150299080 | PRODUCTION METHOD OF CARBONYL COMPOUND - The present invention is to provide a method of producing a carbonyl compound at a higher yield. The method of producing a carbonyl compound according to the present invention produces a carbonyl compound represented by general formula (I) by subjecting a compound represented by general formula (II) to dealkoxycarbonylation in the presence of a hydrogen halide salt of tertiary amine. | 10-22-2015 |
| 568347000 | Oxy containing reactant | 3 |
| 20090187046 | Process to Produce Prostratin and Structural or Functional Analogs Thereof - This invention concerns a process to convert a hydroxyl group (bold in R | 07-23-2009 |
| 20130204046 | HYDRIDE TRANSFER PROCESS FOR KETONE PREPARATION - A hydride transfer process within a reaction between an alcohol and a ketone and in the presence of a heterogeneous catalyst is described. The process can transfer a hydride from an alcohol to a ketone, thus enabling reduction of the ketone and oxidation of the alcohol. Further described, is a process for the simultaneous preparation of cyclohexanone and isopropanol enabling an optimized industrial operation. A mixture of compounds useful for implementing the process and comprising two different ketones and two different alcohols is also described. | 08-08-2013 |
| 20130261343 | METHOD FOR PRODUCING ISOPHORONE - The invention relates to a method for producing isophorone by catalyzed aldol condensation of acetone as an educt, reprocessing the reaction product, hydrolyzing the product stream, and separating into an organic and an aqueous fraction, obtaining isophorone from the organic fraction, distillatively reprocessing the aqueous fraction, and feeding the vapors from the head of the distillative reprocessing apparatus into the hydrolysis apparatus. | 10-03-2013 |
| 568350000 | Gaseous hydrogen reactant or Group IA or IIA light metal containing material utilized | 4 |
| 20110028763 | CYCLOHEXANONE PRODUCTION PROCESS WITH IMPURITIES REMOVAL - The present invention relates to a method for preparing cyclohexanone from phenol in a first process, the first process being a cyclohexanone production process comprising hydrogenating phenol to form a product stream comprising cyclohexanone, phenol and side-products (RSP), including cyclohexanol and undesirable side-product; separating at least part of the product stream having a lower boiling point than cyclohexanone have been removed, into a first fraction comprising cyclohexanone and a second fraction comprising phenol, cyclohexanol and RSP, using distillation; and separating the second fraction into a third fraction, rich in cyclohexanol and comprising RSP, and a fourth fraction, rich in phenol and comprising RSP, using distillation. The invention further relates to an installation for carrying out a method of the invention. | 02-03-2011 |
| 20110172465 | METHOD FOR PRODUCING 3-METHYL-CYCLOPENTADECENONES, METHOD FOR PRODUCING (R)- AND (S)- MUSCONE, AND METHOD FOR PRODUCING OPTICALLY ACTIVE MUSCONE - By intramolecular condensation reaction of 2,15-hexadecanedione in a gaseous phase with a compound of a Group II element of the Periodic Table as a catalyst, 3-methyl-cyclopentadecenones is generated. Magnesium oxide, calcium oxide, or zinc oxide is desirable as the catalyst for the intramolecular condensation reaction. (R)- and (S)-muscone is generated by subjecting 3-methyl-cyclopentadecenones obtained as above to hydrogenation by using a catalyst. Palladium catalyst is desirable as the hydrogenation catalyst. Optically active muscone is generated by separating 3-methyl-cyclopentadecenones into respective components thereof by means of precision distillation and subsequently subjecting the separated 3-methyl-cyclopentadecenones to asymmetric hydrogenation by using an optically active ruthenium complex catalyst. The production methods described above enable easy and economical production of 3-methyl-cyclopentadecenones, (R)- and (S)-muscone, and optically active muscone. | 07-14-2011 |
| 20120178970 | METHOD FOR PRODUCING CYCLOHEXYL ALKYL KETONES - Provided is an industrially superior method for producing cyclohexyl alkyl ketones, which solves the problems in process reduction and in disposal of wastes such as metals. | 07-12-2012 |
| 20130150626 | METHOD FOR HYDROGENATION OF ISO-ALPHA-ACIDS AND TETRAHYDRO-ISO-ALPHA- ACIDS TO HEXAHYDRO-ISO-ALPHA-ACIDS - The invention relates to a process for the production of hexahydro-iso-alpha-acids starting from iso-alpha-acids (or tetrahydro-iso-alpha-acids) in which iso-alpha-acids (or tetrahydro-iso-alpha-acids) are mixed with a heterogeneous ruthenium containing catalyst, that catalyzes the hydrogenation from iso-alpha-acids or tetrahydro-iso-alpha-acids to hexahydro-iso-alpha-acids, either in solvent-free conditions, or in the presence of a solvent phase (e.g. carbon dioxide, water, ethanol or another organ-ic solvent, or mixtures thereof), and in the absence or presence of other hop compounds (such as beta-acids). The resulting mix-ture is then subjected to a temperature at which the iso-alpha-acid (or tetrahydro-iso-alpha-acid) containing reaction medium is sufficiently low in viscosity to allow easy mixing with the heterogeneous ruthenium containing catalyst and held under a hydrogen containing atmosphere (either pure hydrogen gas or mixed with an inert gas) for a reaction tune sufficient to effect high conver-sion of the iso-alpha-acid (or tetrahydro-iso-alpha-acid) reactant into the hexahydro-iso-alpha-acid product. The molar ratio of iso-alpha-acid or tetrahydro-iso-alpha-acid to ruthenium varies between 1:1 and 2000:1. After the hydrogenation process, the hetero-geneous ruthenium containing catalyst can be separated from the hexahydro-iso-alpha-acid product phase by centrifugation, filtra-tion, decantation or other liquid-solid separation techniques. The hydrogenation process can be performed batch-wise or alterna-tively in continuous mode. | 06-13-2013 |
| 568351000 | Nitrogen containing material utilized | 2 |
| 20120310013 | 5-NORBORNENE-2-SPIRO-a-CYCLOALKANONE-a'-SPIRO-2''-5''-NORBORNENE AND METHOD FOR PRODUCING THE SAME - A 5-norbornene-2-spiro-α-cycloalkanone-α′-spiro-2″-5″-norbornene represented by the following general formula (1): | 12-06-2012 |
| 20130338402 | PROCESS FOR PREPARING MACROCYCLIC KETONES - The present invention relates to a process for preparing cyclic compounds having at least eight carbon atoms and at least one keto group, to the cyclic compounds obtained by this process and to the use thereof, in particular as fragrance or for providing a fragrance. | 12-19-2013 |
| 568353000 | Ketone reacted with ketone | 1 |
| 20150045585 | HYDROLYSIS OF THE RESIDUES OBTAINED IN THE PRODUCTION OF ISOPHORONE TO RECOVER ISOPHORONE AND ACETONE - A process for preparing isophorone (3,5,5-trimethyl-2-cyclohexen-1-one) is provided wherein distillation vapors from the work-up of product fractions are recycled to earlier stages of operation of the process. | 02-12-2015 |
