JP2005535455A5 - - Google Patents

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Publication number
JP2005535455A5
JP2005535455A5 JP2005506118A JP2005506118A JP2005535455A5 JP 2005535455 A5 JP2005535455 A5 JP 2005535455A5 JP 2005506118 A JP2005506118 A JP 2005506118A JP 2005506118 A JP2005506118 A JP 2005506118A JP 2005535455 A5 JP2005535455 A5 JP 2005535455A5
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JP
Japan
Prior art keywords
mmol
added
cannula
orange
reaction
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JP2005506118A
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English (en)
Japanese (ja)
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JP2005535455A (ja
JP5101014B2 (ja
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Priority claimed from GBGB0218613.8A external-priority patent/GB0218613D0/en
Priority claimed from GBGB0228018.8A external-priority patent/GB0228018D0/en
Priority claimed from GB0316159A external-priority patent/GB0316159D0/en
Application filed filed Critical
Priority claimed from PCT/GB2003/003419 external-priority patent/WO2004014552A1/en
Publication of JP2005535455A publication Critical patent/JP2005535455A/ja
Publication of JP2005535455A5 publication Critical patent/JP2005535455A5/ja
Application granted granted Critical
Publication of JP5101014B2 publication Critical patent/JP5101014B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2005506118A 2002-08-10 2003-08-06 ホスファアダマンタン触媒系、及びその触媒系を用いたエチレン性不飽和化合物のカルボニル化の方法 Expired - Fee Related JP5101014B2 (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
GBGB0218613.8A GB0218613D0 (en) 2002-08-10 2002-08-10 Process for the carbonylation of ethylenically unsaturated compounds
GB0218613.8 2002-08-10
GB0228018.8 2002-11-30
GBGB0228018.8A GB0228018D0 (en) 2002-11-30 2002-11-30 Carbonylation of ester
GB0316159A GB0316159D0 (en) 2003-07-10 2003-07-10 A catalyst system
GB0316159.3 2003-07-10
PCT/GB2003/003419 WO2004014552A1 (en) 2002-08-10 2003-08-06 A phospha-adamantane (s) catalytic system

Publications (3)

Publication Number Publication Date
JP2005535455A JP2005535455A (ja) 2005-11-24
JP2005535455A5 true JP2005535455A5 (OSRAM) 2007-05-17
JP5101014B2 JP5101014B2 (ja) 2012-12-19

Family

ID=31721066

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2005506118A Expired - Fee Related JP5101014B2 (ja) 2002-08-10 2003-08-06 ホスファアダマンタン触媒系、及びその触媒系を用いたエチレン性不飽和化合物のカルボニル化の方法

Country Status (16)

Country Link
US (1) US7371705B2 (OSRAM)
EP (1) EP1534427B1 (OSRAM)
JP (1) JP5101014B2 (OSRAM)
KR (1) KR101035697B1 (OSRAM)
CN (1) CN1674990B (OSRAM)
AT (1) ATE446140T1 (OSRAM)
AU (1) AU2003259322C1 (OSRAM)
BR (1) BR0313289B1 (OSRAM)
CA (1) CA2493250C (OSRAM)
DE (1) DE60329764D1 (OSRAM)
ES (1) ES2334222T3 (OSRAM)
IN (1) IN227859B (OSRAM)
MY (1) MY139539A (OSRAM)
PL (1) PL374194A1 (OSRAM)
TW (1) TWI301481B (OSRAM)
WO (1) WO2004014552A1 (OSRAM)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007516197A (ja) 2003-07-03 2007-06-21 ルーサイト インターナショナル ユーケー リミテッド エチレン性不飽和化合物のヒドロホルミル化方法
GB0403592D0 (en) 2004-02-18 2004-03-24 Lucite Int Uk Ltd A catalyst system
GB0411951D0 (en) * 2004-05-28 2004-06-30 Lucite Int Uk Ltd Carbonylation of ester
GB0516556D0 (en) 2005-08-12 2005-09-21 Lucite Int Uk Ltd Improved catalyst system
AU2006314268C1 (en) 2005-11-17 2014-01-09 Lucite International Uk Limited Carbonylation of ethylenically unsaturated compounds
GB0607494D0 (en) 2006-04-13 2006-05-24 Lucite Int Uk Ltd Metal complexes
GB2437930A (en) * 2006-05-10 2007-11-14 Lucite Int Uk Ltd Mixing apparatus
US9809611B2 (en) * 2006-12-02 2017-11-07 Lucite International Uk Limited Carbonylation ligands and their use in the carbonylation of ethylenically unsaturated compounds
GB0625518D0 (en) * 2006-12-21 2007-01-31 Lucite Int Uk Ltd Carbonylation of conjugated dienes
GB0812297D0 (en) 2008-07-04 2008-08-13 Lucite Int Uk Ltd Novel carbonylation ligand sand thier use of in the carbonylation of ethylenically unsaturated compounds
GB201000078D0 (en) 2010-01-05 2010-02-17 Lucite Int Uk Ltd Process for the carbonylation of ethylenically unsaturated compounds, novel carbonylation ligands and catalyst systems incorporatng such ligands
WO2016164258A1 (en) * 2015-04-10 2016-10-13 Dow Global Technologies Llc Butadiene telomerization catalyst and preparation thereof
EP3441383B1 (de) * 2017-08-08 2019-12-25 Evonik Operations GmbH Methoxycarbonylierung mit ameisensäure als co-quelle
EP3441384B1 (de) * 2017-08-08 2019-12-25 Evonik Operations GmbH Methoxycarbonylierung mit ameisensäure und methanol
CN111087306B (zh) 2019-12-27 2021-08-03 南京诚志清洁能源有限公司 芳基双齿膦配体组合催化制备有机羧酸酯的方法
CN113999262B (zh) * 2021-12-31 2022-03-29 苏州欣诺科生物科技有限公司 二(1-金刚烷基)环烷基膦配体的制备方法

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4377708A (en) 1977-10-14 1983-03-22 Monsanto Company Hydrocarboxylation of vinyl alkanoates
DE2824010A1 (de) 1978-06-01 1979-12-13 Metallgesellschaft Ag Verfahren zur aufkonzentrierung von verduennter phosphorsaeure
EP0055875B1 (en) 1981-01-06 1986-08-20 Shell Internationale Researchmaatschappij B.V. Process for the carbonylation of olefins
CA1231346A (en) 1982-09-30 1988-01-12 Eit Drent Process for the carbonylation of olefinically unsaturated compounds with a palladium catalyst
GB8531624D0 (en) 1985-12-23 1986-02-05 Shell Int Research Carbonylation of ethylenically unsaturated compounds
GB8605034D0 (en) 1986-02-28 1986-04-09 Shell Int Research Carbonylation of compounds
KR880007426A (ko) 1986-12-24 1988-08-27 오노 알버어스 팔라듐 촉매를 사용한 올레핀형 불포화 화합물의 카르보닐화 방법
GB8705699D0 (en) 1987-03-11 1987-04-15 Shell Int Research Carbonylation of olefinically unsaturated compounds
US4960949A (en) * 1988-12-22 1990-10-02 Eastman Kodak Company Low pressure rhodium catalyzed hydroformylation of olefins
US5158921A (en) 1989-03-03 1992-10-27 Shell Oil Company Carbonylation catalyst and process
CA2034971A1 (en) 1990-02-05 1991-08-06 Eit Drent Carbonylation catalyst system
CA2055628A1 (en) 1990-12-03 1992-06-04 Eit Drent Carbonylation process and catalyst composition
DE69204691T2 (de) 1991-01-15 1996-04-11 Shell Int Research Verfahren zur Karbonylierung von Olefin.
EP0495547B1 (en) 1991-01-15 1996-04-24 Shell Internationale Researchmaatschappij B.V. Carbonylation of olefins
EP0499329B1 (en) 1991-02-15 1994-05-04 Shell Internationale Researchmaatschappij B.V. Carbonylation catalyst system
GB9425911D0 (en) 1994-12-22 1995-02-22 Ici Plc Process for the carbonylation of olefins and catalyst system for use therein
GB9705699D0 (en) 1997-03-19 1997-05-07 Ici Plc Process for the carbonylation of ethylene
GB9717059D0 (en) 1997-08-13 1997-10-15 Ici Plc Method of manufacturing phosphine compound
GB9722733D0 (en) 1997-10-29 1998-10-28 Ici Plc Production of esters
GB9805348D0 (en) 1998-03-16 1998-05-06 Ici Plc Compound
GB9918229D0 (en) * 1999-08-04 1999-10-06 Ici Plc Improvements relating to metal-compound catalysed processes
US6743911B2 (en) * 2000-03-14 2004-06-01 Shell Oil Company Process for the carbonylation of pentenenitrile
US6706912B2 (en) * 2000-03-14 2004-03-16 Shell Oil Company Process for the carbonylation of ethylenically unsaturated compounds
CN100516017C (zh) * 2002-02-19 2009-07-22 国际壳牌研究有限公司 使烯键式不饱和化合物羰基化的方法以及用于该方法的催化剂
JP2007516197A (ja) 2003-07-03 2007-06-21 ルーサイト インターナショナル ユーケー リミテッド エチレン性不飽和化合物のヒドロホルミル化方法

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