JP2014502254A5 - - Google Patents
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- JP2014502254A5 JP2014502254A5 JP2013532821A JP2013532821A JP2014502254A5 JP 2014502254 A5 JP2014502254 A5 JP 2014502254A5 JP 2013532821 A JP2013532821 A JP 2013532821A JP 2013532821 A JP2013532821 A JP 2013532821A JP 2014502254 A5 JP2014502254 A5 JP 2014502254A5
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- JP
- Japan
- Prior art keywords
- ligand
- substituted
- group
- calixarene
- organic phosphine
- 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.)
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- 239000003446 ligand Substances 0.000 claims 15
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 14
- VTJUKNSKBAOEHE-UHFFFAOYSA-N calixarene Chemical compound COC(=O)COC1=C(CC=2C(=C(CC=3C(=C(C4)C=C(C=3)C(C)(C)C)OCC(=O)OC)C=C(C=2)C(C)(C)C)OCC(=O)OC)C=C(C(C)(C)C)C=C1CC1=C(OCC(=O)OC)C4=CC(C(C)(C)C)=C1 VTJUKNSKBAOEHE-UHFFFAOYSA-N 0.000 claims 11
- 239000000203 mixture Substances 0.000 claims 11
- 238000000034 method Methods 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims 7
- 150000001336 alkenes Chemical class 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 229910052723 transition metal Inorganic materials 0.000 claims 4
- 150000003624 transition metals Chemical class 0.000 claims 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical group C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims 3
- 239000003054 catalyst Substances 0.000 claims 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 3
- 238000007037 hydroformylation reaction Methods 0.000 claims 3
- 125000003368 amide group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000000732 arylene group Chemical group 0.000 claims 2
- GQPLZGRPYWLBPW-UHFFFAOYSA-N calix[4]arene Chemical group C1C(C=2)=CC=CC=2CC(C=2)=CC=CC=2CC(C=2)=CC=CC=2CC2=CC=CC1=C2 GQPLZGRPYWLBPW-UHFFFAOYSA-N 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 229930194542 Keto Natural products 0.000 claims 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 claims 1
- 229910017052 cobalt Inorganic materials 0.000 claims 1
- 239000010941 cobalt Substances 0.000 claims 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims 1
- 239000012530 fluid Substances 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 229910052741 iridium Inorganic materials 0.000 claims 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims 1
- 125000000468 ketone group Chemical group 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 239000000376 reactant Substances 0.000 claims 1
- 229910052703 rhodium Inorganic materials 0.000 claims 1
- 239000010948 rhodium Substances 0.000 claims 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims 1
- 229910052707 ruthenium Inorganic materials 0.000 claims 1
- 239000004711 α-olefin Substances 0.000 claims 1
Claims (14)
- カリックスアレーンビスホスファイト配位子及び有機ホスフィン配位子を含んでなる組成物。
- 前記カリックスアレーンビスホスファイト配位子が以下の式で表される、請求項1に記載の組成物:
- 前記カリックスアレーンビスホスファイト配位子が以下の式から選択される、請求項1に記載の組成物:
- 前記有機ホスフィン配位子が以下の式:
P(R)3
(式中、各Rは同じであっても異なってもよく、置換又は非置換のアリール基である)で表されるトリアリールホスフィンである、請求項1に記載の組成物。 - 前記有機ホスフィンがトリフェニルホスフィンである、請求項1に記載の組成物。
- 請求項1に記載の配位子と錯体形成した遷移金属を含んでなる触媒錯体。
- 触媒錯体の存在下で、CO、H2及び少なくとも1種のオレフィンを接触させることを含む方法であって、前記錯体が請求項1に記載のカリックスアレーンビスホスファイト配位子及び有機ホスフィン配位子を含み、少なくとも1種のアルデヒド生成物を形成するのに十分なヒドロホルミル化条件下で行われる、前記方法。
- 成分として遷移金属、カリックスアレーンビスホスファイト配位子及び有機ホスフィン配位子を有する触媒の存在下で、少なくとも1種のアルデヒド生成物を形成するのに十分なヒドロホルミル化条件下で、CO、H2及び少なくとも1種のオレフィンを接触させることを含む方法であって、前記有機ホスフィンの前記触媒金属に対するモル比が150:1より大きく、反応速度が少なくとも0.2g−mol/l−hrである、前記方法。
- ノルマル生成物の分岐生成物に対する比(N/I比)が少なくとも13である、請求項9に記載の方法。
- 前記方法が、反応容器中で行われ、前記遷移金属の濃度が、前記容器中のヒドロホルミル化反応流体の重量を基準にして約100万分の1(ppm)より高く約1,000ppmより低い、請求項9に記載の方法。
- プロセス温度が約−25℃より高く約200℃未満であり、一酸化炭素、水素及びオレフィン性反応物質を含んでなる総ガス圧が約25psia(173kPa)より大きく約2,000psia(14,000kPa)未満であり、前記一酸化炭素の分圧が約15psia(103.4kPa)〜約200psia(1378kPa)であり、前記オレフィンが炭素数2〜30のアキラルなαオレフィン又は炭素数4〜20のアキラルな内部オレフィンであり、一酸化炭素と水素は、H2:COモル比が1:10〜100:1となる量で存在し、前記遷移金属が、ロジウム、コバルト、イリジウム、ルテニウム及びその混合物から選択されるVIII族金属である、請求項9に記載の方法。
- 前記オレフィンがプロピレンであり、前記カリックスアレーンビスホスファイト配位子が請求項4に記載されている通りであり、前記有機ホスフィンがトリフェニルホスフィンであり、前記ノルマル/分岐アルデヒド生成物異性体比が13/1〜20/1である、請求項9に記載の方法。
- カリックスアレーンビスホスファイト配位子の混合物を用いるか、有機ホスフィン配位子の混合物を用いるか、カリックスアレーンビスホスファイト配位子の混合物及び有機ホスフィン配位子の混合物を共に用いる、請求項9に記載の方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US38997210P | 2010-10-05 | 2010-10-05 | |
US61/389,972 | 2010-10-05 | ||
PCT/US2011/052500 WO2012047514A1 (en) | 2010-10-05 | 2011-09-21 | Hydroformylation process |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2015097978A Division JP6077590B2 (ja) | 2010-10-05 | 2015-05-13 | ヒドロホルミル化の方法 |
Publications (2)
Publication Number | Publication Date |
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JP2014502254A JP2014502254A (ja) | 2014-01-30 |
JP2014502254A5 true JP2014502254A5 (ja) | 2014-07-10 |
Family
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Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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JP2013532821A Withdrawn JP2014502254A (ja) | 2010-10-05 | 2011-09-21 | ヒドロホルミル化の方法 |
JP2015097978A Active JP6077590B2 (ja) | 2010-10-05 | 2015-05-13 | ヒドロホルミル化の方法 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
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JP2015097978A Active JP6077590B2 (ja) | 2010-10-05 | 2015-05-13 | ヒドロホルミル化の方法 |
Country Status (6)
Country | Link |
---|---|
US (1) | US8741173B2 (ja) |
EP (1) | EP2624953B1 (ja) |
JP (2) | JP2014502254A (ja) |
CN (1) | CN103153462B (ja) |
WO (1) | WO2012047514A1 (ja) |
ZA (1) | ZA201302026B (ja) |
Families Citing this family (7)
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KR101411307B1 (ko) | 2012-04-12 | 2014-06-24 | 삼성메디슨 주식회사 | 초음파 진단장치 |
CN105384772B (zh) * | 2015-12-18 | 2020-12-18 | 湖南理工学院 | 一种制备全取代杯[8]芳烃磷酸酯衍生物的方法 |
EP3801899A1 (en) * | 2018-05-30 | 2021-04-14 | Dow Technology Investments LLC | Methods for slowing deactivation of a catalyst and/or slowing tetraphosphine ligand usage in hydroformylation processes |
KR20210013703A (ko) * | 2018-05-30 | 2021-02-05 | 다우 테크놀로지 인베스트먼츠 엘엘씨. | 모노포스핀, 테트라포스핀 리간드의 조합을 포함하는 촉매 조성물 및 이를 이용하는 하이드로포밀화 공정 |
EP3802476B1 (en) | 2018-05-30 | 2022-04-13 | Dow Technology Investments LLC | Methods of controlling hydroformylation processes |
US11976017B2 (en) | 2019-12-19 | 2024-05-07 | Dow Technology Investments Llc | Processes for preparing isoprene and mono-olefins comprising at least six carbon atoms |
JPWO2023080071A1 (ja) * | 2021-11-02 | 2023-05-11 |
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2011
- 2011-09-21 WO PCT/US2011/052500 patent/WO2012047514A1/en active Application Filing
- 2011-09-21 US US13/877,386 patent/US8741173B2/en active Active
- 2011-09-21 EP EP11761799.3A patent/EP2624953B1/en active Active
- 2011-09-21 JP JP2013532821A patent/JP2014502254A/ja not_active Withdrawn
- 2011-09-21 CN CN201180048078.5A patent/CN103153462B/zh active Active
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2013
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2015
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