DE69520077D1 - Oxotitankomplexe verwendbar als Katalysatoren für assymetrische Reaktionen insbesondere zur Herstellung von beta-hydroxy-Ketonen oder alpha-hydroxy-Carbonsäureestern - Google Patents

Oxotitankomplexe verwendbar als Katalysatoren für assymetrische Reaktionen insbesondere zur Herstellung von beta-hydroxy-Ketonen oder alpha-hydroxy-Carbonsäureestern

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Publication number
DE69520077D1
DE69520077D1 DE69520077T DE69520077T DE69520077D1 DE 69520077 D1 DE69520077 D1 DE 69520077D1 DE 69520077 T DE69520077 T DE 69520077T DE 69520077 T DE69520077 T DE 69520077T DE 69520077 D1 DE69520077 D1 DE 69520077D1
Authority
DE
Germany
Prior art keywords
hydroxy
ketones
catalysts
beta
alpha
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
DE69520077T
Other languages
English (en)
Other versions
DE69520077T2 (de
Inventor
Takeshi Nakai
Dai Kitamoto
Noboru Sayo
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Takasago International Corp
Original Assignee
Takasago Perfumery Industry Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Application filed by Takasago Perfumery Industry Co filed Critical Takasago Perfumery Industry Co
Application granted granted Critical
Publication of DE69520077D1 publication Critical patent/DE69520077D1/de
Publication of DE69520077T2 publication Critical patent/DE69520077T2/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2226Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/223At least two oxygen atoms present in one at least bidentate or bridging ligand
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2226Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/511Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C67/347Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/003Compounds containing elements of Groups 4 or 14 of the Periodic Table without C-Metal linkages
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/34Other additions, e.g. Monsanto-type carbonylations, addition to 1,2-C=X or 1,2-C-X triplebonds, additions to 1,4-C=C-C=X or 1,4-C=-C-X triple bonds with X, e.g. O, S, NH/N
    • B01J2231/3411,2-additions, e.g. aldol or Knoevenagel condensations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0261Complexes comprising ligands with non-tetrahedral chirality
    • B01J2531/0266Axially chiral or atropisomeric ligands, e.g. bulky biaryls such as donor-substituted binaphthalenes, e.g. "BINAP" or "BINOL"
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/40Complexes comprising metals of Group IV (IVA or IVB) as the central metal
    • B01J2531/46Titanium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2540/00Compositional aspects of coordination complexes or ligands in catalyst systems
    • B01J2540/30Non-coordinating groups comprising sulfur
    • B01J2540/34Sulfonyl groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
DE69520077T 1994-03-11 1995-03-09 Oxotitankomplexe verwendbar als Katalysatoren für assymetrische Reaktionen insbesondere zur Herstellung von beta-hydroxy-Ketonen oder alpha-hydroxy-Carbonsäureestern Expired - Fee Related DE69520077T2 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06760794A JP3337311B2 (ja) 1994-03-11 1994-03-11 新規オキソ−チタン錯体、その製造方法およびその錯体を用いたβ−ヒドロキシケトンまたはα−ヒドロキシカルボン酸エステルの製造方法

Publications (2)

Publication Number Publication Date
DE69520077D1 true DE69520077D1 (de) 2001-03-22
DE69520077T2 DE69520077T2 (de) 2001-06-21

Family

ID=13349799

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69520077T Expired - Fee Related DE69520077T2 (de) 1994-03-11 1995-03-09 Oxotitankomplexe verwendbar als Katalysatoren für assymetrische Reaktionen insbesondere zur Herstellung von beta-hydroxy-Ketonen oder alpha-hydroxy-Carbonsäureestern

Country Status (4)

Country Link
US (3) US5616751A (de)
EP (1) EP0676404B1 (de)
JP (1) JP3337311B2 (de)
DE (1) DE69520077T2 (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6143682A (en) * 1995-06-07 2000-11-07 Exxon Chemical Patents Inc. Bimetallocyclic transition metal catalyst systems
EP0816341A1 (de) 1996-07-04 1998-01-07 F. Hoffmann-La Roche Ag Verfahren zur Herstellung von chiralen Bernsteinsäurederivaten
WO2000056448A1 (en) * 1999-03-19 2000-09-28 Uop Llc Catalyst and process for producing optically active beta amino acids and esters
JP2007106734A (ja) * 2005-10-13 2007-04-26 Tokyo Institute Of Technology 新規な光学活性遷移金属錯体,及びその製造方法
JP5229441B2 (ja) * 2006-03-24 2013-07-03 日産化学工業株式会社 光学活性チタンサラレン化合物の製造方法
KR101642695B1 (ko) * 2007-05-03 2016-07-27 오테라, 인코포레이티드 티타닐의 단량체와 중합체를 함유하는 생성물과 이를 제조하는 방법
WO2016154529A1 (en) 2015-03-26 2016-09-29 Auterra, Inc. Adsorbents and methods of use
US10450516B2 (en) 2016-03-08 2019-10-22 Auterra, Inc. Catalytic caustic desulfonylation

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3134737A (en) * 1960-08-24 1964-05-26 Texaco Inc Novel titanium compound and lubricating composition containing said compound
US3856839A (en) * 1971-01-06 1974-12-24 Gen Electric Alkanedioxy titanium chelates
US4471130A (en) * 1980-08-06 1984-09-11 The Board Of Trustees Of The Leland Stanford Junior University Method for asymmetric epoxidation
US4705764A (en) * 1985-10-03 1987-11-10 Research Development Corporation Of Japan Esterification and/or ester interchange catalyst
AU597042B2 (en) * 1986-04-07 1990-05-24 Ici Australia Limited Enantioselective process for the preparation of a homallyl alcohol
JPS6452786A (en) * 1987-05-21 1989-02-28 Nippon Soda Co Cyclic titanoxane, production thereof and surface-treating agent
US5344948A (en) * 1992-02-25 1994-09-06 Iowa State University Research Foundation, Inc. Single-source molecular organic chemical vapor deposition agents and use
BE1005719A3 (fr) * 1992-03-17 1993-12-28 Solvay Procede de production d'epichlorhydrine.

Also Published As

Publication number Publication date
US5616751A (en) 1997-04-01
EP0676404B1 (de) 2001-02-14
JPH07252277A (ja) 1995-10-03
DE69520077T2 (de) 2001-06-21
US5714624A (en) 1998-02-03
EP0676404A2 (de) 1995-10-11
EP0676404A3 (de) 1996-07-17
JP3337311B2 (ja) 2002-10-21
US5705678A (en) 1998-01-06

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