JP5893646B2 - Z選択的オレフィンメタセシス触媒及びその合成手順 - Google Patents

Z選択的オレフィンメタセシス触媒及びその合成手順 Download PDF

Info

Publication number
JP5893646B2
JP5893646B2 JP2013549616A JP2013549616A JP5893646B2 JP 5893646 B2 JP5893646 B2 JP 5893646B2 JP 2013549616 A JP2013549616 A JP 2013549616A JP 2013549616 A JP2013549616 A JP 2013549616A JP 5893646 B2 JP5893646 B2 JP 5893646B2
Authority
JP
Japan
Prior art keywords
substituted
heteroatom
aryl
hydrocarbyl
alkyl
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
JP2013549616A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014503356A5 (https=
JP2014503356A (ja
Inventor
浩司 遠藤
浩司 遠藤
キース ケイツ、ベンジャミン
キース ケイツ、ベンジャミン
ベントン ハーバート、マイルス
ベントン ハーバート、マイルス
ラシクラル パテル、パレスマ
ラシクラル パテル、パレスマ
ハワード グラッブス、ロバート
ハワード グラッブス、ロバート
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.)
California Institute of Technology
Original Assignee
California Institute of Technology
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 California Institute of Technology filed Critical California Institute of Technology
Publication of JP2014503356A publication Critical patent/JP2014503356A/ja
Publication of JP2014503356A5 publication Critical patent/JP2014503356A5/ja
Application granted granted Critical
Publication of JP5893646B2 publication Critical patent/JP5893646B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

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
    • 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
    • B01J31/2282Unsaturated compounds used as ligands
    • B01J31/2295Cyclic compounds, e.g. cyclopentadienyls
    • 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
    • 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
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • 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
    • B01J31/2265Carbenes or carbynes, i.e.(image)
    • B01J31/2269Heterocyclic carbenes
    • B01J31/2273Heterocyclic carbenes with only nitrogen as heteroatomic ring members, e.g. 1,3-diarylimidazoline-2-ylidenes
    • 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
    • B01J31/2265Carbenes or carbynes, i.e.(image)
    • B01J31/2278Complexes comprising two carbene ligands differing from each other, e.g. Grubbs second generation catalysts
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • 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
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/0046Ruthenium compounds
    • 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
    • B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/54Metathesis reactions, e.g. olefin metathesis
    • B01J2231/543Metathesis reactions, e.g. olefin metathesis alkene metathesis
    • 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
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/22Organic complexes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
JP2013549616A 2011-01-14 2012-01-17 Z選択的オレフィンメタセシス触媒及びその合成手順 Expired - Fee Related JP5893646B2 (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US201161432849P 2011-01-14 2011-01-14
US61/432,849 2011-01-14
US201161433949P 2011-01-18 2011-01-18
US61/433,949 2011-01-18
US201161515262P 2011-08-04 2011-08-04
US61/515,262 2011-08-04
PCT/US2012/021609 WO2012097379A2 (en) 2011-01-14 2012-01-17 Z-selective olefin metathesis catalysts and their synthetic procedure

Publications (3)

Publication Number Publication Date
JP2014503356A JP2014503356A (ja) 2014-02-13
JP2014503356A5 JP2014503356A5 (https=) 2015-02-26
JP5893646B2 true JP5893646B2 (ja) 2016-03-23

Family

ID=46507707

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2013549616A Expired - Fee Related JP5893646B2 (ja) 2011-01-14 2012-01-17 Z選択的オレフィンメタセシス触媒及びその合成手順

Country Status (13)

Country Link
US (1) US9597674B2 (https=)
EP (1) EP2663398B1 (https=)
JP (1) JP5893646B2 (https=)
KR (1) KR101835170B1 (https=)
CN (1) CN103402628B (https=)
AU (1) AU2012206966B2 (https=)
BR (1) BR112013017938B1 (https=)
CA (1) CA2824518C (https=)
IL (1) IL227432A (https=)
PL (1) PL2663398T3 (https=)
SG (1) SG191980A1 (https=)
WO (1) WO2012097379A2 (https=)
ZA (2) ZA201305726B (https=)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2838359A4 (en) 2012-03-05 2015-12-09 California Inst Of Techn SYNTHESIS OF Z-OLEFIN-CONTAINING PHEROMONES OF LEPIDOPTERA INSECTS
JP6092379B2 (ja) 2012-06-29 2017-03-08 アペイロン シンセシス エス アー 金属錯体、その適用、及びメタセシス反応の実施方法
US9147844B2 (en) 2012-08-01 2015-09-29 California Institute Of Technology Solvent-free enyne metathesis polymerization
US9234985B2 (en) 2012-08-01 2016-01-12 California Institute Of Technology Birefringent polymer brush structures formed by surface initiated ring-opening metathesis polymerization
BR112015013580A2 (pt) 2012-12-12 2017-07-11 California Inst Of Techn catalisador de metátese z-seletiva
US9758445B2 (en) 2013-04-09 2017-09-12 Materia, Inc. Preparation of surfactants via cross-metathesis
US9663440B2 (en) 2013-04-09 2017-05-30 Materia, Inc. Cross metathesis of poly-branched poly-olefins
ES2699416T3 (es) 2013-04-09 2019-02-11 Materia Inc Preparación de tensioactivos mediante metátesis cruzada
US20160101414A1 (en) * 2013-05-15 2016-04-14 California Institute Of Technology Highly z-selective and enantioselective ring opening/cross metathesis catalyzed by a resolved stereogenic-at-ru complex
EP3008078B1 (en) 2013-06-12 2018-12-19 Trustees of Boston College Catalysts for efficient z-selective metathesis
WO2016014954A1 (en) * 2014-07-25 2016-01-28 California Institute Of Technology Tandem z-selective metathesis / dihydroxylation
PL3353187T3 (pl) * 2015-09-24 2021-11-22 Umicore Ag & Co. Kg Katalizatory metatezy olefin na bazie karbenu metalu
KR20180116238A (ko) 2015-12-10 2018-10-24 우미코레 아게 운트 코 카게 올레핀 복분해 촉매
CN114106057B (zh) * 2016-10-19 2023-06-23 优美科股份公司及两合公司 Ru亚烷基络合物的合成与表征
US10320390B1 (en) 2016-11-17 2019-06-11 X Development Llc Field programmable gate array including coupled lookup tables
WO2018220088A1 (en) 2017-05-30 2018-12-06 Ximo Ag Methods of making olefinic e- and z-isomers
EP3762143A1 (en) * 2018-03-09 2021-01-13 PPG Industries Ohio Inc. Compounds for coordinating with a metal, compositions containing such compounds, and methods of catalyzing reactions
CN112119055A (zh) * 2018-05-15 2020-12-22 加利福尼亚技术学院 通过立体保留性复分解全合成前列腺素j天然产物
US11939410B2 (en) * 2018-06-29 2024-03-26 Apeiron Synthesis S.A. Organoruthenium complexes as precatalysts for olefin metathesis
CN114206889A (zh) * 2019-07-17 2022-03-18 加利福尼亚技术学院 Z选择性烯烃复分解催化剂的新合成
EP4069667A1 (en) * 2020-03-05 2022-10-12 Firmenich SA Process for preparing perfuming intermediate
CN115298191A (zh) * 2020-03-13 2022-11-04 伊利诺伊大学评议会 催化氢化硅烷化的方法
CN114478166B (zh) * 2020-10-26 2024-09-27 中国石油天然气股份有限公司 一种制备端烯烃的方法
CN118056617A (zh) * 2022-11-15 2024-05-21 中国石油天然气股份有限公司 一种用于1-己烯自歧化的负载型催化剂及其制备方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5312940A (en) 1992-04-03 1994-05-17 California Institute Of Technology Ruthenium and osmium metal carbene complexes for olefin metathesis polymerization
US6284852B1 (en) 1997-10-30 2001-09-04 California Institute Of Technology Acid activation of ruthenium metathesis catalysts and living ROMP metathesis polymerization in water
JP3943015B2 (ja) 2000-08-10 2007-07-11 トラスティーズ オブ ボストン カレッジ リサイクル可能メタセシス触媒
US6620955B1 (en) 2001-11-15 2003-09-16 Richard L. Pederson Chelating carbene ligand precursors and their use in the synthesis of metathesis catalysts
CN1659172B (zh) * 2002-04-05 2012-08-01 加州理工学院 直接被吸电子基团取代的烯烃使用过渡金属卡宾催化剂的交叉-易位
AU2005252276B2 (en) * 2004-06-09 2010-10-14 Uti Limited Partnership Transition metal carbene complexes containing a cationic substituent as catalysts of olefin metathesis reactions
FR2878246B1 (fr) 2004-11-23 2007-03-30 Inst Francais Du Petrole Procede de co-production d'olefines et d'esters par ethenolyse de corps gras insatures dans des liquides ioniques non-aqueux
WO2007003135A1 (en) * 2005-07-04 2007-01-11 Zheng-Yun Zhan Ruthenium complex ligand, ruthenium complex, carried ruthenium complex catalyst and the preparing methods and the use thereof
US8877936B2 (en) * 2008-04-09 2014-11-04 California Institute Of Technology Ruthenium olefin metathesis catalysts bearing N-heterocyclic carbene ligands with substituted backbone
EP2255877B1 (en) * 2009-05-07 2014-09-24 Umicore AG & Co. KG Method for preparation of ruthenium-based metathesis catalysts with chelating alkylidene ligands

Also Published As

Publication number Publication date
US20140106960A1 (en) 2014-04-17
IL227432A0 (en) 2013-09-30
JP2014503356A (ja) 2014-02-13
EP2663398A4 (en) 2014-07-23
CA2824518A1 (en) 2012-07-19
BR112013017938A2 (pt) 2018-11-27
BR112013017938B1 (pt) 2019-10-15
ZA201408071B (en) 2019-06-26
EP2663398B1 (en) 2018-07-18
US9597674B2 (en) 2017-03-21
WO2012097379A2 (en) 2012-07-19
KR101835170B1 (ko) 2018-03-06
WO2012097379A3 (en) 2012-10-11
ZA201305726B (en) 2018-12-19
CA2824518C (en) 2019-03-26
PL2663398T3 (pl) 2019-01-31
AU2012206966B2 (en) 2016-11-17
KR20140021995A (ko) 2014-02-21
IL227432A (en) 2017-12-31
CN103402628A (zh) 2013-11-20
SG191980A1 (en) 2013-08-30
CN103402628B (zh) 2015-12-23
EP2663398A2 (en) 2013-11-20

Similar Documents

Publication Publication Date Title
JP5893646B2 (ja) Z選択的オレフィンメタセシス触媒及びその合成手順
AU2012206966A1 (en) Z-selective olefin metathesis catalysts and their synthetic procedure
CN101243098B (zh) 作为烯烃易位反应催化剂的含阳离子取代基的过渡金属卡宾配合物
EP3386936B1 (en) Olefin metathesis catalysts
JP5622711B2 (ja) N−複素環カルベンリガンドを含有する高活性潜伏オレフィン複分解触媒
RU2553993C2 (ru) Каталитический комплекс для реакций метатезиса олефинов, способ его приготовления и его применение
JP5619724B2 (ja) 置換された骨格を有するn−ヘテロ環状カルベンリガンドを有するルテニウムオレフィン複分解触媒
JP4409087B2 (ja) ルテニウム及びオスミウムメタセシス触媒のシッフ塩基誘導体
JP5522941B2 (ja) 有機金属ルテニウム錯体および関連する四置換および別の嵩高いオレフィンの製造方法
CN102834175B (zh) 带有螯合亚烷基配体的钌基卡宾催化剂的制备方法
JP2012525960A (ja) キレート化アルキリデン配位子を有するルテニウムベースのメタセシス触媒の製造方法
US20170022232A1 (en) Method for in-situ formation of metathesis catalysts
Jung et al. A cationic allenylideneruthenium (II) complex with two bulky hemilabile phosphine ligands
Römer et al. One-step synthesis of Mo (0) and W (0) bis (dinitrogen) complexes with the linear tetraphosphine ligand prP 4: stereoselective formation of cis-[M (N2) 2 (rac-prP4)] and trans-[M (N2) 2 (meso-prP4)]; M= Mo, W
Gao et al. Cyclometallation reactions of a three-coordinate cobalt (I) complex bearing a nonsymmetric N-heterocyclic carbene ligand
Jung et al. A series of ruthenium (ii) complexes containing the bulky, functionalized trialkylphosphines t Bu 2 PCH 2 XC 6 H 5 as ligands
CN114106057B (zh) Ru亚烷基络合物的合成与表征
JP2003190807A (ja) オレフィンメタセシス触媒
Cinellu Gold–Alkene Complexes
CN101090915A (zh) 含有n-杂环卡宾配体的潜伏的高活性烯烃置换催化剂
Tancu Monofunctional and dendritic schiff base (N, N′) ruthenium carbene

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20150107

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20150107

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20150629

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20150730

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20151009

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20160129

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: 20160212

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20160201

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20160224

R150 Certificate of patent or registration of utility model

Ref document number: 5893646

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees