JP4538796B2 - 酵素触媒反応によるフェノール性カルボン酸誘導体の製造方法 - Google Patents

酵素触媒反応によるフェノール性カルボン酸誘導体の製造方法 Download PDF

Info

Publication number
JP4538796B2
JP4538796B2 JP2004542420A JP2004542420A JP4538796B2 JP 4538796 B2 JP4538796 B2 JP 4538796B2 JP 2004542420 A JP2004542420 A JP 2004542420A JP 2004542420 A JP2004542420 A JP 2004542420A JP 4538796 B2 JP4538796 B2 JP 4538796B2
Authority
JP
Japan
Prior art keywords
group
carbon atoms
alkyl
formula
phenyl
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
JP2004542420A
Other languages
English (en)
Japanese (ja)
Other versions
JP2006501831A5 (enExample
JP2006501831A (ja
Inventor
エールライン，ラインホルト
バイシュ，ガブリエーレ
シェーニング，カイ−ウヴェ
シュミット，イェミマ
フランツィスカ マイヤー，ザンドラ
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.)
BASF Schweiz AG
Original Assignee
Ciba Holding AG
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 Ciba Holding AG filed Critical Ciba Holding AG
Publication of JP2006501831A publication Critical patent/JP2006501831A/ja
Publication of JP2006501831A5 publication Critical patent/JP2006501831A5/ja
Application granted granted Critical
Publication of JP4538796B2 publication Critical patent/JP4538796B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/62—Carboxylic acid esters
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • C12P7/42—Hydroxy-carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P11/00—Preparation of sulfur-containing organic compounds
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/02—Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/10—Nitrogen as only ring hetero atom
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/22—Preparation of oxygen-containing organic compounds containing a hydroxy group aromatic
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
    • C12P7/6436—Fatty acid esters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
JP2004542420A 2002-10-10 2003-10-02 酵素触媒反応によるフェノール性カルボン酸誘導体の製造方法 Expired - Fee Related JP4538796B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP02405869 2002-10-10
PCT/EP2003/010967 WO2004033699A1 (en) 2002-10-10 2003-10-02 Process for the preparation of phenolic carboxylic acid derivatives by enzymatic catalysis

Publications (3)

Publication Number Publication Date
JP2006501831A JP2006501831A (ja) 2006-01-19
JP2006501831A5 JP2006501831A5 (enExample) 2006-11-24
JP4538796B2 true JP4538796B2 (ja) 2010-09-08

Family

ID=32088102

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004542420A Expired - Fee Related JP4538796B2 (ja) 2002-10-10 2003-10-02 酵素触媒反応によるフェノール性カルボン酸誘導体の製造方法

Country Status (8)

Country Link
US (1) US7507853B2 (enExample)
EP (1) EP1549752A1 (enExample)
JP (1) JP4538796B2 (enExample)
KR (1) KR101058446B1 (enExample)
AU (1) AU2003293598A1 (enExample)
CA (1) CA2499813A1 (enExample)
TW (1) TWI321154B (enExample)
WO (1) WO2004033699A1 (enExample)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005514496A (ja) * 2002-01-04 2005-05-19 マサチューセッツ、ゼネラル、ホスピタル 溶融体を下回る温度で調製した残留フリーラジカルが減少した高弾性率架橋ポリエチレン
DE102004019472A1 (de) * 2004-04-22 2005-11-17 Bayer Healthcare Ag Phenylacetamide
UA97127C2 (uk) * 2006-12-06 2012-01-10 Бандж Ойлз, Инк. Спосіб безперервної ферментативної обробки композиції, що містить ліпід, та система для його здійснення
EP2529632B1 (de) 2011-05-31 2013-08-28 Symrise AG Zimtsäureamide als würzige Geschmacksstoffe
DE102017220555A1 (de) 2017-11-17 2019-05-23 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Verbindungen mit stabilisierender Wirkung, Verfahren zu deren Herstellung, Zusammensetzung enthaltend diese stabilisierenden Verbindungen, Verfahren zur Stabilisierung einer organischen Komponente sowie Verwendung von stabilisierenden Verbindungen
CN107954863A (zh) * 2017-12-13 2018-04-24 新乡市瑞丰新材料股份有限公司 酚酯型抗氧剂的制备方法
CN111205207A (zh) * 2020-03-17 2020-05-29 山东小驴快跑信息技术有限公司 一种抗氧剂及应用
CN113429360B (zh) * 2021-08-11 2023-03-17 山东省临沂市三丰化工有限公司 一种固体抗氧剂的制备方法
CN114539175A (zh) * 2022-01-19 2022-05-27 江苏富比亚化学品有限公司 一种紫外吸收剂uv-384-2的合成方法
US20250171407A1 (en) 2022-02-22 2025-05-29 Basf Se Ultraviolet absorber
CN114671777B (zh) * 2022-03-18 2023-09-19 天津利安隆新材料股份有限公司 酰胺类抗氧剂的制备方法
CN115927491A (zh) * 2022-08-01 2023-04-07 新乡市瑞丰新材料股份有限公司 一种己二醇双[3-3,5-二叔丁基-4-羟基苯基]丙酸酯的制备方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4594444A (en) * 1983-12-22 1986-06-10 Ciba-Geigy Corporation Process for the preparation of sterically hindered hydroxyphenylcarboxylic acid esters
EP0808818B1 (en) * 1996-05-23 2000-09-20 Ciba SC Holding AG Process for the preparation of substituted hydroxy-hydrocinnamate esters
BR9714168A (pt) * 1996-12-20 2000-04-25 Cia Speciality Chemicals Holdi Catalisadores de trasesterificação fixados em materiais de suporte sólidos.
IT1303821B1 (it) 1998-12-04 2001-02-23 Great Lakes Chemical Italia Procedimento per la preparazione di diacilidrazine simmetriche.
JP2003506065A (ja) * 1999-08-05 2003-02-18 ノボ ノルディスク アクティーゼルスカブ 置換された３−フェニル−プロパン酸エステル及び置換された３−フェニル−プロパン酸の調製の方法
US6346236B1 (en) * 2000-03-28 2002-02-12 The United States Of America As Represented By The Secretary Of Agriculture Sunscreens from vegetable oil and plant phenols

Also Published As

Publication number Publication date
AU2003293598A1 (en) 2004-05-04
CA2499813A1 (en) 2004-04-22
EP1549752A1 (en) 2005-07-06
KR101058446B1 (ko) 2011-08-24
TWI321154B (en) 2010-03-01
WO2004033699A1 (en) 2004-04-22
US7507853B2 (en) 2009-03-24
TW200413534A (en) 2004-08-01
US20060110807A1 (en) 2006-05-25
KR20050053753A (ko) 2005-06-08
JP2006501831A (ja) 2006-01-19

Similar Documents

Publication Publication Date Title
JP4538796B2 (ja) 酵素触媒反応によるフェノール性カルボン酸誘導体の製造方法
US5604120A (en) Method for producing optically active endo-2-norborneols
IE65881B1 (en) Method for preparing optically active 3-phenylglycidic acid esters
US7005281B2 (en) Enzymatic process for preparing organosilicon group containing photoinitiators
US6406912B1 (en) Method for enzymatic enantiomer-separation of 3(r)- and 3(s)-hydroxy-1-methyl-4-(2,4,6-trimethoxyphenyl)-1,2,3,6-tetrahydro-pyridine or its carboxylic acid esters
CA2578298A1 (en) Enantioselective biotransformation for preparation of protein tyrosine kinase inhibitor intermediates
BE1007297A3 (nl) Werkwijze voor de bereiding van optisch aktieve alcoholen en esters, en alcoholen en esters toegepast en bereid in dergelijke werkwijzen.
Arosio et al. Chemo‐enzymatic dynamic kinetic resolution of amino acid thioesters
US6121025A (en) Process for producing optically active 3-quinuclidinol derivatives
US20100159538A1 (en) Method for the chemoenzymatic production of fatty acid esters
US7138256B2 (en) Processes for preparing conjugated linoleic acid from conjugated linoleic acid esters
AU617344B2 (en) A process for the enzymatic preparation of optically active phosphorus-containing functional acetic acid derivatives
CA2321450A1 (en) Process for producing (r)-2-hydroxy-1-phenoxypropane derivative
JP2639651B2 (ja) 光学活性カルボン酸及びその対掌体エステルの製造法
JP4565672B2 (ja) 光学活性β−シアノイソ酪酸類及びその製造方法
JPS6094091A (ja) 光学活性カルボン酸エステルの製造法
JPS6012992A (ja) 光学活性カルボン酸の製造法
JP4392812B2 (ja) 新規光学活性４−アミノ−２−メチル酪酸誘導体及びその製造方法
KR19980701914A (ko) 효소 촉매된 아실화 반응에 의한 헤테로 원자 치환된 1급 및 2급 아민 라세미체의 분리 방법
JP2004113049A (ja) 常温溶融塩中での生体触媒によるエステル交換反応方法
JPH05192188A (ja) 光学活性な置換酪酸またはそのエステル誘導体の製造法
JP2008079526A (ja) ジカルボン酸モノエステルの製造方法
JP2007117034A (ja) 光学活性ニペコチン酸化合物の製造方法
MXPA00007811A (en) Method for enzymatic enantiomer-separation of 3(r)- and 3(s)-hydroxy-1- methyl-4-(2,4, 6-trimethoxyphenyl)-1, 2,3,6- tetrahydro-pyridine or its carboxylic acid esters
JP2009263341A (ja) 光学活性ニペコチン酸エステル誘導体の製造法

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20060929

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20060929

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20091021

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20100121

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20100128

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100222

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20100331

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100423

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20100526

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20100610

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130702

Year of fee payment: 3

LAPS Cancellation because of no payment of annual fees