JP2017517477A5 - - Google Patents
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- Publication number
- JP2017517477A5 JP2017517477A5 JP2016557062A JP2016557062A JP2017517477A5 JP 2017517477 A5 JP2017517477 A5 JP 2017517477A5 JP 2016557062 A JP2016557062 A JP 2016557062A JP 2016557062 A JP2016557062 A JP 2016557062A JP 2017517477 A5 JP2017517477 A5 JP 2017517477A5
- Authority
- JP
- Japan
- Prior art keywords
- dimer
- hetero
- homo
- formula
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 claims 22
- 239000000833 heterodimer Substances 0.000 claims 15
- 150000001336 alkenes Chemical group 0.000 claims 10
- 239000000710 homodimer Substances 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 5
- 239000003054 catalyst Substances 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 125000004404 heteroalkyl group Chemical group 0.000 claims 3
- 125000001072 heteroaryl group Chemical group 0.000 claims 3
- 241000402754 Erythranthe moschata Species 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- 125000005011 alkyl ether group Chemical group 0.000 claims 2
- 125000001118 alkylidene group Chemical group 0.000 claims 2
- 125000005587 carbonate group Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 239000000539 dimer Substances 0.000 claims 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical group [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 2
- 125000004185 ester group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 239000000543 intermediate Substances 0.000 claims 2
- 239000003446 ligand Substances 0.000 claims 2
- 229910052750 molybdenum Inorganic materials 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 238000007363 ring formation reaction Methods 0.000 claims 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 2
- 238000005809 transesterification reaction Methods 0.000 claims 2
- 229910052721 tungsten Inorganic materials 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical group [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims 1
- 241000270666 Testudines Species 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
- 238000004821 distillation Methods 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 230000007062 hydrolysis Effects 0.000 claims 1
- 238000006460 hydrolysis reaction Methods 0.000 claims 1
- 238000005649 metathesis reaction Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000011733 molybdenum Substances 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims 1
- 125000005353 silylalkyl group Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 229910052723 transition metal Inorganic materials 0.000 claims 1
- 150000003624 transition metals Chemical class 0.000 claims 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims 1
- 239000010937 tungsten Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB201404468A GB201404468D0 (en) | 2014-03-13 | 2014-03-13 | Process |
| GB1404468.9 | 2014-03-13 | ||
| PCT/EP2015/055343 WO2015136093A1 (en) | 2014-03-13 | 2015-03-13 | Process involving cross metathesis of olefins |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020024151A Division JP7051918B2 (ja) | 2014-03-13 | 2020-02-17 | オレフィンのクロスメタセシスを含む方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017517477A JP2017517477A (ja) | 2017-06-29 |
| JP2017517477A5 true JP2017517477A5 (enExample) | 2018-04-19 |
| JP6738736B2 JP6738736B2 (ja) | 2020-08-12 |
Family
ID=50634692
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016557062A Active JP6738736B2 (ja) | 2014-03-13 | 2015-03-13 | オレフィンのクロスメタセシスを含む方法 |
| JP2020024151A Active JP7051918B2 (ja) | 2014-03-13 | 2020-02-17 | オレフィンのクロスメタセシスを含む方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020024151A Active JP7051918B2 (ja) | 2014-03-13 | 2020-02-17 | オレフィンのクロスメタセシスを含む方法 |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US10144720B2 (enExample) |
| EP (1) | EP3116848B1 (enExample) |
| JP (2) | JP6738736B2 (enExample) |
| CN (1) | CN106103403B (enExample) |
| BR (1) | BR112016020155B1 (enExample) |
| ES (1) | ES2972431T3 (enExample) |
| GB (1) | GB201404468D0 (enExample) |
| MX (1) | MX385080B (enExample) |
| SG (1) | SG11201606977QA (enExample) |
| WO (1) | WO2015136093A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201404468D0 (en) * | 2014-03-13 | 2014-04-30 | Givaudan Sa | Process |
| EP3215516B1 (en) * | 2014-11-05 | 2020-01-08 | Massachusetts Institute Of Technology | Metathesis catalysts and methods thereof |
| EP3237372B1 (en) * | 2014-12-26 | 2021-01-20 | Kao Corporation | Method for producing omega-hydroxy fatty acid ester and precursor compound thereof |
| AU2016357756B2 (en) | 2015-11-18 | 2021-09-30 | Provivi, Inc. | Production of fatty olefin derivatives via olefin metathesis |
| GB201604110D0 (en) * | 2016-03-10 | 2016-04-20 | Givaudan Sa | Preparation of macrocyclic lactones |
| US10774035B2 (en) * | 2016-09-23 | 2020-09-15 | Umicore Ag & Co. Kg | Preparation of amino acids and amino acid derivatives |
| US10844036B2 (en) | 2016-12-05 | 2020-11-24 | Agan Aroma & Fine Chemicals Ltd. | Processes for obtaining purified unsaturated macrocyclic compounds |
| JP7153937B2 (ja) | 2017-02-17 | 2022-10-17 | プロビビ インコーポレイテッド | オレフィンメタセシスによるフェロモンおよび関連材料の合成方法 |
| US11161104B2 (en) * | 2018-02-13 | 2021-11-02 | Umicore Ag & Co. Kg | Reactions of olefin derivatives in the presence of methathesis catalysts |
| EP3768691A1 (en) * | 2018-03-22 | 2021-01-27 | Verbio Vereinigte BioEnergie AG | Tetraphenylphenoxy tungsten oxo alkylidene complexes, methods of making same and use thereof |
| EP3778843A4 (en) * | 2018-04-02 | 2021-12-22 | Kao Corporation | MUSK-TYPE COMPOSITION |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4014902A (en) * | 1976-06-09 | 1977-03-29 | International Flavors & Fragrances Inc. | Intermediate in the process for the preparation of trans-Δ9 -isoambrettolide |
| US6271015B1 (en) | 1995-06-12 | 2001-08-07 | The Scripps Research Institute | Fatty-acid amide hydrolase |
| JP2866622B2 (ja) | 1996-09-17 | 1999-03-08 | 花王株式会社 | 新規含フッ素化合物及びこれを含有する潤滑剤並びに磁気記録媒体 |
| US5936100A (en) | 1996-12-16 | 1999-08-10 | Studiengesellschaft Kohle Mbh | Synthesis of functionalized macrocycles by ring closing metathesis |
| EP0908455B1 (de) | 1997-10-09 | 2002-07-10 | Givaudan SA | Macrocyclen |
| JP4943612B2 (ja) | 1999-11-18 | 2012-05-30 | エル ペダーソン リチャード | フェロモン又はその成分のメタセシス合成方法 |
| JP2009538337A (ja) * | 2006-05-22 | 2009-11-05 | ニューヨーク・ユニバーシティ | Ｔｈ−１プロフィールが亢進したＣ−糖脂質 |
| US8362311B2 (en) * | 2009-09-30 | 2013-01-29 | Massachusetts Institute Of Technology | Highly Z-selective olefins metathesis |
| WO2014018578A1 (en) * | 2012-07-24 | 2014-01-30 | Heliae Development, Llc | Methods of converting mixtures of palmitoleic and oleic acid esters to high value products |
| GB201404468D0 (en) * | 2014-03-13 | 2014-04-30 | Givaudan Sa | Process |
-
2014
- 2014-03-13 GB GB201404468A patent/GB201404468D0/en not_active Ceased
-
2015
- 2015-03-13 ES ES15709519T patent/ES2972431T3/es active Active
- 2015-03-13 SG SG11201606977QA patent/SG11201606977QA/en unknown
- 2015-03-13 CN CN201580013580.0A patent/CN106103403B/zh active Active
- 2015-03-13 WO PCT/EP2015/055343 patent/WO2015136093A1/en not_active Ceased
- 2015-03-13 MX MX2016011286A patent/MX385080B/es unknown
- 2015-03-13 US US15/120,802 patent/US10144720B2/en active Active
- 2015-03-13 JP JP2016557062A patent/JP6738736B2/ja active Active
- 2015-03-13 BR BR112016020155-8A patent/BR112016020155B1/pt active IP Right Grant
- 2015-03-13 EP EP15709519.1A patent/EP3116848B1/en active Active
-
2018
- 2018-11-30 US US16/205,952 patent/US20190100504A1/en not_active Abandoned
-
2020
- 2020-02-17 JP JP2020024151A patent/JP7051918B2/ja active Active
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