DE69903880T2 - Oxidationskatalysator-System und dessen Verwendung zur Herstellung von Ketoisophoron - Google Patents

Oxidationskatalysator-System und dessen Verwendung zur Herstellung von Ketoisophoron

Info

Publication number
DE69903880T2
DE69903880T2 DE69903880T DE69903880T DE69903880T2 DE 69903880 T2 DE69903880 T2 DE 69903880T2 DE 69903880 T DE69903880 T DE 69903880T DE 69903880 T DE69903880 T DE 69903880T DE 69903880 T2 DE69903880 T2 DE 69903880T2
Authority
DE
Germany
Prior art keywords
ketoisophorone
production
catalyst system
oxidation catalyst
oxidation
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
DE69903880T
Other languages
English (en)
Other versions
DE69903880D1 (de
Inventor
Ikuo Takahashi
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.)
Daicel Corp
Original Assignee
Daicel Chemical Industries Ltd
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
Application filed by Daicel Chemical Industries Ltd filed Critical Daicel Chemical Industries Ltd
Publication of DE69903880D1 publication Critical patent/DE69903880D1/de
Application granted granted Critical
Publication of DE69903880T2 publication Critical patent/DE69903880T2/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208—Oxygen, e.g. acetylacetonates
    • B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/2243—At least one oxygen and one nitrogen atom present as complexing atoms in an at least bidentate or bridging ligand
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
    • C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/70—Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0238—Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
    • B01J2531/0241—Rigid ligands, e.g. extended sp2-carbon frameworks or geminal di- or trisubstitution
    • B01J2531/0252—Salen ligands or analogues, e.g. derived from ethylenediamine and salicylaldehyde
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/50—Complexes comprising metals of Group V (VA or VB) as the central metal
    • B01J2531/56—Vanadium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/70—Complexes comprising metals of Group VII (VIIB) as the central metal
    • B01J2531/72—Manganese
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84—Metals of the iron group
    • B01J2531/842—Iron
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84—Metals of the iron group
    • B01J2531/845—Cobalt

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
DE69903880T 1998-06-01 1999-05-31 Oxidationskatalysator-System und dessen Verwendung zur Herstellung von Ketoisophoron Expired - Fee Related DE69903880T2 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10151644A JPH11342340A (ja) 1998-06-01 1998-06-01 酸化触媒系及びそれを用いたケトイソホロンの製造方法

Publications (2)

Publication Number Publication Date
DE69903880D1 DE69903880D1 (de) 2002-12-19
DE69903880T2 true DE69903880T2 (de) 2003-03-27

Family

ID=15523076

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69903880T Expired - Fee Related DE69903880T2 (de) 1998-06-01 1999-05-31 Oxidationskatalysator-System und dessen Verwendung zur Herstellung von Ketoisophoron

Country Status (4)

Country Link
US (1) US6166261A (de)
EP (1) EP0962440B1 (de)
JP (1) JPH11342340A (de)
DE (1) DE69903880T2 (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020055657A1 (en) * 1998-07-16 2002-05-09 Daicel Chemical Industries,Ltd. Process and apparatus for producing ketoisophorone
JP2000034255A (ja) 1998-07-16 2000-02-02 Daicel Chem Ind Ltd ケトイソホロンの製造方法および製造装置
KR100718770B1 (ko) * 2001-12-07 2007-05-16 에스케이 주식회사 케토-이소포론의 제조방법
CN1186125C (zh) * 2002-06-18 2005-01-26 中国科学院成都有机化学研究所 用于氧化偶联萘酚的手性催化剂
AU2002349706A1 (en) * 2002-11-25 2004-06-18 Maruzen Petrochemical Co., Ltd. Process for producing carbonyl compound
WO2005009613A1 (ja) * 2003-07-25 2005-02-03 Asahi Kasei Chemicals Corporation 酸化触媒
EP2623199B1 (de) * 2010-10-01 2018-11-07 Ube Industries, Ltd. Oxidationskatalysator für eine kohlenwasserstoffverbindung sowie verfahren und vorrichtung zur erzeugung eines oxids aus der kohlenwasserstoffverbindung mithilfe dieses katalysators
CN110721696B (zh) * 2019-10-01 2020-06-05 山东新和成维生素有限公司 一种采用钙钛矿型复合氧化物催化合成茶香酮的方法
CN110773228B (zh) * 2019-10-12 2022-07-12 万华化学集团股份有限公司 催化剂的制备方法及催化剂在制备β-异佛尔酮中的应用

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL6410417A (de) * 1964-09-08 1966-03-09
CH559156A5 (de) * 1972-11-16 1975-02-28 Firmenich & Cie
CH586173A5 (de) * 1973-12-07 1977-03-31 Firmenich & Cie
JPS5125316A (en) * 1974-08-24 1976-03-01 Omoto Constr Co Ltd Izutsu mataha senkanno pc burotsukunyorukariheki
FR2303785A1 (fr) * 1975-03-11 1976-10-08 Rhone Poulenc Ind Procede d'oxydation de cetones b-ethyleniques
JPS61191645A (ja) * 1985-02-20 1986-08-26 Sagami Chem Res Center オキソホロンの製造方法
JPS63122644A (ja) * 1986-11-11 1988-05-26 Soda Koryo Kk ３，５，５−トリメチルシクロヘキサ−２−エン−１，４−ジオンの製造方法
JPS6490150A (en) * 1987-09-30 1989-04-06 Soda Aromatic Production of 3,5,5-trimethylcyclohex-2-ene-1,4-dione
JPH01175955A (ja) * 1987-12-28 1989-07-12 Soda Koryo Kk ３，５，５−トリメチルシクロヘキサ−２−エン−１，４−ジオンの製造方法
DE19619570A1 (de) * 1996-05-15 1997-11-20 Degussa Verfahren zur Herstellung von Ketoisophoron
JP5530696B2 (ja) * 2009-10-27 2014-06-25 株式会社明治 プラズマローゲン型リン脂質

Also Published As

Publication number Publication date
DE69903880D1 (de) 2002-12-19
EP0962440B1 (de) 2002-11-13
EP0962440A1 (de) 1999-12-08
US6166261A (en) 2000-12-26
JPH11342340A (ja) 1999-12-14

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