序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
241 VERFAHREN ZUR METALLORGANISCHEN HERSTELLUNG ORGANISCHER ZWISCHENPRODUKTE MIT KOHLENSTOFF-HETEROATOM-BINDUNGEN BER DIE DEPROTONIERUNG VON HETEROATOMEN EP03794905.4 2003-08-21 EP1537125A1 2005-06-08 MEUDT, Andreas; LEHNEMANN, Bernd; ERBES, Michael; FORSTINGER, Klaus
The invention relates to a method for binding heteroatom-carbon bonds. According to said method, a lithium compound (II) is first generated by reacting aliphatic or aromatic halogen compounds (I) with lithium metal, said compound is then used for the deprotonation of the compounds (III) or (V). The lithium salts of formulas (IV) or (VI) obtained by said deprotonation are subsequently reacted with suitable carbon electrophiles (equation I), said process binding the heteroatom-carbon bond and forming the products (VIII) or (VIII), (equation I).
242 PROCEDE D'OXYDATION D'HYDROCARBURES EP02727704.5 2002-04-30 EP1390338A1 2004-02-25 FACHE, Eric; SIMONATO, Jean-Pierre
The invention relates to a method for oxidising hydrocarbons, particularly branched or non-branched saturated aliphatic hydrocarbons, cycloaliphatic or alkyl aromatic hydrocarbons, into alcohol, ketone and/or acid, polyacid compounds. More specifically, the invention relates to the oxidation, using an oxidising agent containing molecular oxygen, of cyclohexane into cyclohexanol, cyclohexanone and/or adipic acid. The oxidation is carried out in the presence of a catalytic system comprising a catalyst based on at least one metal compound and a co-catalyst comprising an imide function such as N-bromosuccinimide, N-bromomaleimide, N-bromohexahydrophtalimide, N,N'-dibromocyclohexanetetracarboximide, N-bromophtalimide, N-bromotrimellitimide, N,N'-dibromopyromellitimide.
243 PROCESS FOR THE PREPARATION OF ALCOHOL DERIVATIVES EP00110209.4 2000-05-17 EP1057822B1 2003-02-12 Uno, Mitsuru; Okutsu, Munehisa; Kitsuki, Tomohito
244 CATALYTIC OXIDATION OF ORGANIC SUBSTRATES BY TRANSITION METAL COMPLEXES IN ORGANIC SOLVENT MEDIA EXPANDED BY SUPERCRITICAL OR SUBCRITICAL CARBON DIOXIDE EP01928364.7 2001-04-03 EP1268383A1 2003-01-02 SUBRAMANIAM, Bala; BUSCH, Daryle, H.; MUSIE, Ghezai, T.; WEI, Ming
Improved oxidation methods are provided wherein a reaction mixture comprising a substrate to be oxidized (e.g., phenols, alkenes) and an oxidation catalyst (typically dispersed in an organic solvent system) is supplemented with a compressed gas which expands the reaction mixture, thus accelerating the oxidation reaction. In preferred practice pressurized subcritical or supercritical carbon dioxide is used as the expanding gas, which is introduced into the reaction mixture together with an oxidizing agent. The inventive methods improve the substrate conversion and product selectivity by increasing the solubility of the oxidizing agent in the reaction mixture.
245 VERFAHREN ZUR OXIDATION VON KOHLENWASSERSTOFFEN EP01936129.4 2001-03-22 EP1268367A2 2003-01-02 KÜHNLE, Adolf; DUDA, Mark; SHELDON, Roger, Arthur; SASIDHARAN, Manickam; ARENDS, Isabella, W., C., E.; SCHIFFER, Thomas; FRIES, Guido; KIRCHHOFF, Jochen; JOST, Carsten, Dr.
The invention relates to a method for oxidizing substrates such as hydrocarbons, waxes or soot. The method involves the use of a compound of formula (I) in which: R?1 and R2¿ represent H, an aliphatic or aromatic alkoxy radical, carboxyl radical, alkoxycarbonyl radical or hydrocarbon radical, each having 1 to 20 hydrocarbon atoms, SO¿3?H, NH2, OH, F, Cl, Br, I and/or NO2, whereby R?1 and R2¿ designate identical or different radicals or R?1 and R2¿ can be linked to one another via a covalent bonding; Q¿1? and Q2 represent C, CH, N, CR?5¿, each being the same or different; X and Z represent C, S, CH¿2?, each being the same or different; Y represents O and OH; k = 0, 1, 2; l = 0, 1, 2; m = 1 to 3, and; R?5¿ represents one of the meanings of R1. Said compound is used as a catalyst in the presence of a radical initiator, whereby the molar ratio of the catalyst to the hydrocarbon is less than 10 mol %. Peroxy compounds or azo compounds can be used as the radical initiator. Preferred substrates are aliphatic or aromatic hydrocarbons.
246 PROCESS FOR CATALYZING THE OXIDATION OF ORGANIC COMPOUNDS EP00960420.8 2000-08-09 EP1208069A1 2002-05-29 BERNARDELLI, Patrick
Oxidation of organic compounds is catalyzed by addition of a catalytic amount of a metalloporphyrin in a non-reactive aprotic solvent.
247 Process for the catalytic selective oxidation of a hydrocarbon compound in presence of mesoporous zeolite EP01121417.8 2001-09-07 EP1195368A2 2002-04-10 Schmidt, Iver; Brorson, Michael; Jacobsen, Claus J.H.

Processes applying mesoporous titanium containing zeolite based catalysts for selective oxidation or epoxidation of hydrocarbons by peroxides.

248 Process for producing carbonyl or hydroxy compound EP01119369.5 2001-08-10 EP1188735A1 2002-03-20 Hagiya, Koji; Takano, Naoyuki; Kurihara, Akio

There are disclosed are a method for producing at least one compound selected from a carbonyl compound and a hydroxy adduct compound by an oxidative cleavage or addition reaction of an olefinic double bond of an olefin compound,

   which contains

      reacting an olefin compound with hydrogen peroxide, utilizing as a catalyst, at least one member selected from

  • (a) tungsten,
  • (b) molybdenum, or
  • (c) a tungsten or molybdenum metal compound containing
    • (ia) tungsten or (ib) molybdenum and
    • (ii) an element of Group IIIb, IVb, Vb or VIb excluding oxygen, and
a catalyst composition.

249 Method for starting up reactor EP01306660.0 2001-08-03 EP1180508A1 2002-02-20 Hirao, Harunori; Matsumoto, Yukihiro; Nakahara, Sei; Suzuki, Kunihiko

In the reaction of catalytic gas phase oxidation induced by the supply of at least a raw material to be oxidized and a molecular oxygen-containing gas to a reactor for catalytic gas phase oxidation, a method for starting up the reactor for catalytic gas phase oxidation is disclosed which is characterized by causing the raw material and the molecular oxygen-containing gas to pass a range in which the concentration of the raw material is less than the lower explosion limit of the raw material and the concentration of oxygen is not less than the limiting oxygen concentration, but excluding the concentration of the raw material of 0 vol.%. The method enables the reactor to be started up economically and safely by avoiding the explosion range induced by the composition of a raw material and a molecular oxygen-containing gas supplied to the reactor and decreasing the amount of a diluting gas to be supplied.

250 VERFAHREN ZUR OXIDATION EINER MINDESTENS EINE C-C-DOPPELBINDUNG AUFWEISENDEN ORGANISCHEN VERBINDUNG EP98929426.9 1998-06-05 EP0986526B1 2002-01-30 GROSCH, Georg, Heinrich; MÜLLER, Ulrich; WALCH, Andreas; RIEBER, Norbert; FISCHER, Martin; QUAISER, Stefan; HARDER, Wolfgang; ELLER, Karsten; BASSLER, Peter; WENZEL, Anne; KAIBEL, Gerd; STAMMER, Achim; HENKELMANN, Jochem; BÖTTCHER, Arnd; TELES, Joaquim, Henrique; SCHULZ, Michael; TREIBER, Gert
The invention relates to a method for oxidizing an organic compound containing at least one C-C double bond or a mixture of two or more thereof, comprising the following steps: (I) production of a hydroperoxide; (II) reaction of an organic compound containing at least one C-C double bond or a mixture of two or more thereof with the hydroperoxide produced in step (I) in the presence of a zeolitic catalyst; (III) regeneration of the at least partially deactivated zeolitic catalyst used in step (II) and (IV) reaction according to step (II) using a zeolitic catalyst which contains the regenerated catalyst from step (III).
251 Process for preparing alcohol derivatives EP00110209.4 2000-05-17 EP1057822A3 2000-12-13 Uno, Mitsuru; Okutsu, Munehisa; Kitsuki, Tomohito

The present invention provides a process for preparing an alcohol derivative, where the alcohol derivative is an ester, acetal, ketal, ether, or alkyl glycoside, by reacting an alcohol with a carbonyl compound, alcohol, olefin, epoxy compound or saccharide, where C2-4 vicinal alkylene oxides are excluded, in the presence of (A) an aluminum alkoxide and (B) sulfuric acid or phosphoric acid.

252 PROCESS FOR THE SELECTIVE OXIDATION OF ORGANIC COMPOUNDS EP98965958.6 1998-11-12 EP1056683A2 2000-12-06 SINGH, Prahlad, R.; TERCHO, Gerald, P.; WENTZ, Jack, N., Jr.; OLEWINE, Keith, R.
A process for oxidizing organic compounds is disclosed. Hydrogen peroxide is used to oxidize an oxidizable organic substrate in the presence of a silica-modified titania/silica-containing catalyst. A method for preparing a catalyst using a copolymer of diethoxysilane and ethyl titanate is also disclosed.
253 Process for the selective oxidation of compounds EP96103929.4 1996-03-13 EP0735014B1 2000-08-09 Lee, Ross Albert
254 VERFAHREN ZUR OXIDATION EINER MINDESTENS EINE C-C-DOPPELBINDUNG AUFWEISENDEN ORGANISCHEN VERBINDUNG EP98929426.9 1998-06-05 EP0986526A1 2000-03-22 GROSCH, Georg, Heinrich; MÜLLER, Ulrich; WALCH, Andreas; RIEBER, Norbert; FISCHER, Martin; QUAISER, Stefan; HARDER, Wolfgang; ELLER, Karsten; BASSLER, Peter; WENZEL, Anne; KAIBEL, Gerd; STAMMER, Achim; HENKELMANN, Jochem; BÖTTCHER, Arnd; TELES, Joaquim, Henrique; SCHULZ, Michael; TREIBER, Gert
The invention relates to a method for oxidizing an organic compound containing at least one C-C double bond or a mixture of two or more thereof, comprising the following steps: (I) production of a hydroperoxide; (II) reaction of an organic compound containing at least one C-C double bond or a mixture of two or more thereof with the hydroperoxide produced in step (I) in the presence of a zeolitic catalyst; (III) regeneration of the at least partially deactivated zeolitic catalyst used in step (II) and (IV) reaction according to step (II) using a zeolitic catalyst which contains the regenerated catalyst from step (III).
255 CATALYSTS AND THEIR USE IN OXIDATION OF SATURED HYDROCARBONS EP93917640.0 1993-07-23 EP0651674B1 1999-01-13 HUYBRECHTS, Diane, Renata, Cornelia; BUSKENS, Philip, Luc; MATHYS, Georges, Marie, Karel; MARTENS, Luc, Roger, Marc
256 Verfahren zur Addition von Hydroxylgruppen enthaltenden Verbindungen an Alkine oder Allene EP98110001.9 1998-06-02 EP0887330A1 1998-12-30 Teles, Joaquim Henrique, Dr.; Rieber, Norbert, Dr.; Breuer, Klaus, Dr.; Demuth, Dirk, Dr.; Hibst, Hartmut, Prof.Dr.; Hagemeyer, Alfred, Dr.

Verfahren zur Herstellung von Verbindungen der Formeln I bzw. II in denen R1 Wasserstoff oder einen aliphatischen, cycloaliphatischen, araliphatischen, aromatischen oder heterocyclischen Rest oder einen Acylrest bedeutet, wobei diese Reste weitere Substituenten, die nicht mit Acetylenen oder Allenen reagieren, tragen können und die Reste R unabhängig voneinander für Wasserstoff oder aliphatische, cycloaliphatische, araliphatische, aromatische oder heterocyclische Reste stehen, die unter Bildung eines Ringes miteinander verbunden sein können und m für 0 oder 1 steht, durch Addition von Verbindungen der Formel III



        R1OH     III



an Acetylene oder Allene der Formeln IV bzw. V



        R―C≡C―R     IV



wobei R1 und R die oben angegebenen Bedeutungen haben, in der Gasphase bei erhöhter Temperatur in Gegenwart eines heterogenen, ein Silikat enthaltenden Katalysators, bei dem man einen Katalysator verwendet, der als aktiven Bestandteil ein durch Ausfällung in wäßriger Lösung aus einer löslichen Silizium- und Zinkverbindung erhältliches Zinksilikat enthält oder aus diesem besteht, wobei das Zinksilikat

  • a) ein im wesentlichen röntgenamorphes Zinksilikat der Formel VI,



            ZnaSicOa+2c-0,5e(OH)e.fH2O     VI,



    in der e die Werte 0 bis zur Summe aus 2a + 2c bedeutet und das Verhältnis a/c 1 bis 3,5 und f/a 0 bis 200 beträgt und/oder
  • b) ein kristallines Zinksilikat mit der Struktur von Hemimorphit der Formel Zn4Si2O7(OH)2·2H2O ist.

257 Low thickness antifragmentation plates EP97114419.1 1997-08-21 EP0826490A3 1998-11-18 Stasi, Alberto Luca; Stanco, Donato

Multilayer transparent, antireflex, coloured or opaline plates, with smooth or embossed surfaces, optionally thermouldable with external layers in acrylic polymers, low thickness, in the range of 1.5 up to lower thicknesses of 10 mm, by employing one or more polymeric continuous films which have the property to have elastic modulus lower than the one of PMMA of at least 30%, and/or elongation at break higher than at least 40%, measured by the test according to ISO 527 for plates or films, placed inside the panel.

258 Verfahren zur selektiven Oxidation aromatischer Verbindungen EP95108050.6 1995-05-26 EP0686618B1 1998-01-14 Herrmann, Wolfgang Anton, Prof. Dr.; Galamba Correia, Joao Domingos; Fischer, Richard Walter, Dr.
259 Metal phthalocyanine oxidation catalysts EP93302295.6 1993-03-25 EP0564169B1 1997-05-14 Ellis, Paul E., Jr.; Lyons, James E.
260 Process for the production of partial oxidation products EP96304591.9 1996-06-20 EP0749950A1 1996-12-27 Acharya, Divyanshu R.; Tamhankar, Satish S.

A petrochemical (i.e. a hydrocarbon derivative) is produced by the vapour phase reaction of a hydrocarbon with air in the presence of a suitable catalyst. The petrochemical is removed from the reactor effluent, and part or all of the remaining petrochemical-free gas stream is passed through a hydrocarbon-selective adsorbent, which adsorbs hydrocarbon from the gas stream, leaving a hydrocarbon-depleted waste gas. Hydrocarbon is purged from the adsorbent with air, and the air-hydrocarbon mixture is recycled to the partial oxidation reactor. The purge air, and preferably both the purge air and the petrochemical-free gas stream are dried by passage through beds of zeolite 3A prior to being introduced into the hydrocarbon-selective adsorbent, and the beds of zeolite 3A are regenerated by passing heated hydrocarbon-depleted waste gas therethrough.

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