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ATE120742T1 - Verfahren zur herstellung von e-caprolacton. - Google Patents

Verfahren zur herstellung von e-caprolacton.

Info

Publication number
ATE120742T1
ATE120742T1 AT91303594T AT91303594T ATE120742T1 AT E120742 T1 ATE120742 T1 AT E120742T1 AT 91303594 T AT91303594 T AT 91303594T AT 91303594 T AT91303594 T AT 91303594T AT E120742 T1 ATE120742 T1 AT E120742T1
Authority
AT
Austria
Prior art keywords
mole
caprolactone
cyclohexanone
hydrogen peroxide
less
Prior art date
Application number
AT91303594T
Other languages
English (en)
Inventor
Yukio C O Ube Chemical F Inaba
Kogushi
Yohsuke C O Ube Chemical Ueno
Takafumi C O Ube Chem Hirakawa
Kogushi Oaza
Suzuo C O Ube Chemic Takiguchi
Original Assignee
Atochem Elf Sa
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 Atochem Elf Sa filed Critical Atochem Elf Sa
Application granted granted Critical
Publication of ATE120742T1 publication Critical patent/ATE120742T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D315/00Heterocyclic compounds containing rings having one oxygen atom as the only ring hetero atom according to more than one of groups C07D303/00 - C07D313/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00Preparation of peroxy compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00Preparation of peroxy compounds
    • C07C407/003Separation; Purification; Stabilisation; Use of additives
    • C07C407/006Stabilisation; Use of additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyrane Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
AT91303594T 1990-04-25 1991-04-22 Verfahren zur herstellung von e-caprolacton. ATE120742T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2107674A JPH0798816B2 (ja) 1990-04-25 1990-04-25 ε―カプロラクトンの製造法

Publications (1)

Publication Number Publication Date
ATE120742T1 true ATE120742T1 (de) 1995-04-15

Family

ID=14465118

Family Applications (1)

Application Number Title Priority Date Filing Date
AT91303594T ATE120742T1 (de) 1990-04-25 1991-04-22 Verfahren zur herstellung von e-caprolacton.

Country Status (7)

Country Link
US (1) US5250707A (de)
EP (1) EP0454397B1 (de)
JP (1) JPH0798816B2 (de)
CN (1) CN1035379C (de)
AT (1) ATE120742T1 (de)
CA (1) CA2040270A1 (de)
DE (1) DE69108600T2 (de)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0974581A4 (de) * 1997-09-16 2002-01-02 Daicel Chem Verfahren zur herstellung von peroxysäure im gleichgewicht und verfahren zur herstellung von lacton
JP2004143047A (ja) * 2002-10-22 2004-05-20 Daicel Chem Ind Ltd ε−カプロラクトンの製造方法
JP2005139110A (ja) * 2003-11-06 2005-06-02 Ecology Maximum Co Ltd ε−カプロラクトンの製造方法、並びに、ε−カプロラクトンを用いたポリカプロラクトンの製造方法
JP4297152B2 (ja) 2006-10-06 2009-07-15 トヨタ自動車株式会社 車両前部構造
US8871807B2 (en) 2008-03-28 2014-10-28 Ecolab Usa Inc. Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids
US8809392B2 (en) 2008-03-28 2014-08-19 Ecolab Usa Inc. Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents
CN102105443B (zh) 2008-03-28 2014-05-28 埃科莱布有限公司 磺基过氧羧酸、它们的制备和用作漂白剂和抗微生物剂的方法
CN102584776A (zh) * 2011-01-12 2012-07-18 中国石油化工集团公司 一种制备ε-己内酯的方法
CN102584775B (zh) * 2011-01-12 2015-04-22 中国石油化工集团公司 制备ε-己内酯的方法
CN102304117A (zh) * 2011-09-19 2012-01-04 武汉理工大学 一种合成ε-己内酯的方法
US9321664B2 (en) * 2011-12-20 2016-04-26 Ecolab Usa Inc. Stable percarboxylic acid compositions and uses thereof
US9242879B2 (en) 2012-03-30 2016-01-26 Ecolab Usa Inc. Use of peracetic acid/hydrogen peroxide and peroxide-reducing agents for treatment of drilling fluids, frac fluids, flowback water and disposal water
US20140256811A1 (en) 2013-03-05 2014-09-11 Ecolab Usa Inc. Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids
CN104003972A (zh) * 2014-04-28 2014-08-27 安徽红太阳新材料有限公司 一种制备己内酯的方法
CN104130234A (zh) * 2014-07-25 2014-11-05 南京红太阳新材料有限公司 一种制备己内酯的方法
US10172351B2 (en) 2015-09-04 2019-01-08 Ecolab Usa Inc. Performic acid on-site generator and formulator
CN105315442A (zh) * 2015-12-01 2016-02-10 仇颖超 一种淀粉改性聚己内酯塑料材料的制备方法
GB2548137A (en) * 2016-03-09 2017-09-13 Perstorp Ab Production equipment (I) for production of a caprolactone
GB2548138A (en) * 2016-03-09 2017-09-13 Perstorp Ab Production equipment (II) for production of a caprolactone
CN107163018A (zh) * 2017-06-23 2017-09-15 中山大学惠州研究院 一种分离ε‑己内酯的精馏方法
WO2020041545A1 (en) 2018-08-22 2020-02-27 Ecolab Usa Inc. Hydrogen peroxide and peracid stabilization with molecules based on a pyridine carboxylic acid at c-3, -4 or -5
WO2021026410A1 (en) 2019-08-07 2021-02-11 Ecolab Usa Inc. Polymeric and solid-supported chelators for stabilization of peracid-containing compositions
CN111763192B (zh) * 2020-07-14 2023-09-12 湖南瑞源石化股份有限公司 一种ε-己内酯的制备方法及其装置
CN115490623B (zh) * 2021-06-18 2024-08-30 中国石油化工股份有限公司 合成无水过氧有机酸的方法和合成ε-己内酯的方法
CN114835669A (zh) * 2022-03-23 2022-08-02 华东理工大学 高纯度ε-己内酯的微流控合成方法
CN115812713B (zh) * 2022-11-29 2024-03-29 湖南聚仁新材料股份公司 消毒剂和己内酯生产过程中联产过氧羧酸消毒剂的方法

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3064008A (en) * 1962-11-13 I i i i i i
US2914556A (en) * 1956-04-13 1959-11-24 Union Carbide Corp Preparation of lactone adducts
US3189619A (en) * 1962-09-25 1965-06-15 Exxon Research Engineering Co Synthesis of carpolactone
US3317563A (en) * 1963-12-26 1967-05-02 Celanese Corp Preparation of epsilon-caprolactone
FR1474098A (fr) * 1966-01-25 1967-03-24 Electro Chimie Soc D Procédé de préparation d'epsilon-caprolactone
FR1474903A (fr) * 1966-02-12 1967-03-31 Electrochimie Soc Procédé de préparation d'epsiloncaprolactone
GB1140184A (en) * 1967-06-13 1969-01-15 Chisso Corp Process for manufacturing e-caprolactone
US3624258A (en) * 1969-03-22 1971-11-30 Teijin Ltd Process for the preparation of {68 -caprolactone
DE2038455A1 (de) * 1970-08-01 1972-02-10 Bayer Ag Verfahren zur Herstellung von epsilon-Caprolacton
US3781350A (en) * 1971-07-09 1973-12-25 Teijin Ltd Process for preparation of omega-hydroxy saturated aliphatic monocarboxylic acids
US3825570A (en) * 1971-11-02 1974-07-23 Teijin Ltd Process for the preparation of epsilon-caprolactone
US4183863A (en) * 1978-04-18 1980-01-15 Union Carbide Corporation Conversion of cyclohexanol to ε-caprolactone
DE2920436A1 (de) * 1979-05-19 1980-12-04 Bayer Ag Verfahren zur herstellung von epsilon -caprolacton
DE2934659A1 (de) * 1979-08-28 1981-03-19 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung von sehr reinem epsilon -caprolacton
FR2500453A1 (fr) * 1981-02-20 1982-08-27 Ugine Kuhlmann Procede d'obtention de l'epsilon-caprolactone
FR2519985A1 (fr) * 1982-01-15 1983-07-22 Ugine Kuhlmann Procede perfectionne de fabrication de l'e-caprolactone
JPH0237919B2 (ja) * 1983-05-04 1990-08-28 Mitsubishi Chem Ind Kapurorakutonnoseizohoho
JPS61200120A (ja) * 1985-03-01 1986-09-04 Nippon Shokubai Kagaku Kogyo Co Ltd ラクトン変性化合物の製造方法
DE3823213A1 (de) * 1988-07-08 1990-01-11 Basf Ag Verfahren zur herstellung von caprolacton

Also Published As

Publication number Publication date
US5250707A (en) 1993-10-05
EP0454397A1 (de) 1991-10-30
CN1035379C (zh) 1997-07-09
EP0454397B1 (de) 1995-04-05
CA2040270A1 (en) 1991-10-26
DE69108600D1 (de) 1995-05-11
DE69108600T2 (de) 1996-01-11
JPH0798816B2 (ja) 1995-10-25
CN1071923A (zh) 1993-05-12
JPH049378A (ja) 1992-01-14

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Legal Events

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