JP2010513502A5 - - Google Patents
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- Publication number
- JP2010513502A5 JP2010513502A5 JP2009542869A JP2009542869A JP2010513502A5 JP 2010513502 A5 JP2010513502 A5 JP 2010513502A5 JP 2009542869 A JP2009542869 A JP 2009542869A JP 2009542869 A JP2009542869 A JP 2009542869A JP 2010513502 A5 JP2010513502 A5 JP 2010513502A5
- Authority
- JP
- Japan
- Prior art keywords
- dehydrogenation catalyst
- group
- formula
- compound
- hydrocarbyl group
- 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.)
- Abandoned
Links
- 238000000034 method Methods 0.000 claims 10
- 150000001875 compounds Chemical class 0.000 claims 7
- 239000003054 catalyst Substances 0.000 claims 6
- 238000006356 dehydrogenation reaction Methods 0.000 claims 6
- 229910052751 metal Inorganic materials 0.000 claims 6
- 239000002184 metal Substances 0.000 claims 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 5
- 239000007800 oxidant agent Substances 0.000 claims 5
- 230000001590 oxidative effect Effects 0.000 claims 5
- -1 potassium ferricyanide Chemical compound 0.000 claims 5
- 150000003839 salts Chemical class 0.000 claims 5
- 239000000126 substance Substances 0.000 claims 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims 4
- 229920000642 polymer Polymers 0.000 claims 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 3
- 239000003880 polar aprotic solvent Substances 0.000 claims 3
- 239000011541 reaction mixture Substances 0.000 claims 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 2
- HZNVUJQVZSTENZ-UHFFFAOYSA-N 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(C#N)=C(C#N)C1=O HZNVUJQVZSTENZ-UHFFFAOYSA-N 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims 1
- 229910020175 SiOH Inorganic materials 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 229910021536 Zeolite Inorganic materials 0.000 claims 1
- IKWTVSLWAPBBKU-UHFFFAOYSA-N a1010_sial Chemical compound O=[As]O[As]=O IKWTVSLWAPBBKU-UHFFFAOYSA-N 0.000 claims 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 1
- 229910000413 arsenic oxide Inorganic materials 0.000 claims 1
- 229960002594 arsenic trioxide Drugs 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims 1
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims 1
- 239000003610 charcoal Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 229910000428 cobalt oxide Inorganic materials 0.000 claims 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 claims 1
- 239000000571 coke Substances 0.000 claims 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 1
- 229910021472 group 8 element Inorganic materials 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 239000002638 heterogeneous catalyst Substances 0.000 claims 1
- 239000002815 homogeneous catalyst Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 229910000476 molybdenum oxide Inorganic materials 0.000 claims 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 claims 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 230000000737 periodic effect Effects 0.000 claims 1
- 229910052711 selenium Inorganic materials 0.000 claims 1
- 239000011669 selenium Substances 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 230000002194 synthesizing effect Effects 0.000 claims 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
- 229910001930 tungsten oxide Inorganic materials 0.000 claims 1
- 239000010457 zeolite Substances 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87657706P | 2006-12-21 | 2006-12-21 | |
| PCT/US2007/025816 WO2008082509A2 (en) | 2006-12-21 | 2007-12-18 | Process for the synthesis of diaminopyridines from glutaronitriles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010513502A JP2010513502A (ja) | 2010-04-30 |
| JP2010513502A5 true JP2010513502A5 (cg-RX-API-DMAC7.html) | 2011-01-13 |
Family
ID=39582778
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009542869A Abandoned JP2010513502A (ja) | 2006-12-21 | 2007-12-18 | グルタロニトリルからジアミノピリジンを合成する方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8022167B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2111393A2 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2010513502A (cg-RX-API-DMAC7.html) |
| KR (1) | KR20090091348A (cg-RX-API-DMAC7.html) |
| CN (1) | CN101563325A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2008082509A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2125737A2 (en) * | 2006-12-21 | 2009-12-02 | E. I. Du Pont de Nemours and Company | Process for the synthesis of 2,6-diaminopyridines from glutarimidines |
| US7999057B2 (en) * | 2008-07-08 | 2011-08-16 | E. I. Du Pont De Nemours And Company | Gas-phase process for the synthesis of diaminopyridines from glutaronitriles |
| JP2012512889A (ja) | 2008-12-18 | 2012-06-07 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | グルタロニトリルからジアミノピリジンを合成するための連続液相法 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2816879A (en) * | 1951-11-15 | 1957-12-17 | Du Pont | Process for preparing polyureas utilizing immiscible phases |
| GB1135462A (en) * | 1966-05-13 | 1968-12-04 | Ici Ltd | Aromatic polyamides |
| US3966652A (en) * | 1974-11-11 | 1976-06-29 | International Harvester Company | Method of making foamed copolyimides and product obtained therefrom |
| DE2519529B2 (de) * | 1975-05-02 | 1979-08-09 | Dynamit Nobel Ag, 5210 Troisdorf | Verfahren zur Herstellung von 3-Methylpyridin |
| US4068050A (en) * | 1976-05-17 | 1978-01-10 | Cpc International Inc. | Difunctional terminated macromolecular monomers and condensation copolymers produced therefrom |
| US4051140A (en) * | 1976-07-01 | 1977-09-27 | The Lummus Company | Preparation of pyridines and nicotinonitrile from piperidines |
| EP0062264A3 (de) * | 1981-03-31 | 1983-06-01 | Lonza Ag | Verfahren zur Herstellung von Amino-Pyridinen |
| US4451642A (en) * | 1981-05-21 | 1984-05-29 | E. I. Du Pont De Nemours And Company | Bis(aminoneopentyl) aromatics and polyamides derived therefrom |
| FR2514772B1 (fr) * | 1981-10-19 | 1985-09-06 | Inst Francais Du Petrole | Compositions reactives de polyimides thermostables presentant une solubilite elevee et leurs utilisations |
| US5028713A (en) * | 1983-12-08 | 1991-07-02 | The Standard Oil Company | Ammoxidation of methyl substituted heteroaromatics to make heteroaromatic nitriles |
| US4603207A (en) * | 1985-10-24 | 1986-07-29 | The Standard Oil Company | Conversion of a mixture of 3-methylpyridine and 3-methylpiperidine to 3-cyanopyridine |
| US4876348A (en) * | 1985-10-29 | 1989-10-24 | The Standard Oil Company | Process for making 3-cyanopyridine |
| US4737571A (en) * | 1986-01-17 | 1988-04-12 | E. I. Du Pont De Nemours And Company | Preparation of aromatic polyamide with solvent system comprising N-alkyl substituted amide and quaternary ammonium compound |
| US5061784A (en) * | 1990-08-06 | 1991-10-29 | Hoechst Celanese Corporation | Polymers prepared from 4,4'-bis(3,4-dicarboxyphenyl) hexafluoroisopropyl) diphenyl dianhydride |
| US5066809A (en) * | 1990-09-27 | 1991-11-19 | The Standard Oil Company | Preparation of 3-methylpyridine from 2-methylglutaronitrile |
| JP3527740B2 (ja) | 1993-04-28 | 2004-05-17 | マゼラン システムズ インターナショナル，エルエルシー | ピリドビスイミダゾールに基く剛直なロッドポリマー |
| US5693227A (en) * | 1994-11-17 | 1997-12-02 | Ionics, Incorporated | Catalyst mediated method of interfacial polymerization on a microporous support, and polymers, fibers, films and membranes made by such method |
| NL1000360C2 (nl) * | 1995-05-15 | 1996-11-18 | Akzo Nobel Nv | Werkwijze ter bereiding van pyridine-2, 6-diamines |
| US6118003A (en) * | 1998-01-29 | 2000-09-12 | Reilly Industries, Inc. | Processes for producing 3-cyanopyridine from 2-methyl-1,5-pentanediamine |
| DE60029085T8 (de) | 1999-10-21 | 2007-05-16 | Teijin Ltd. | Verfahren zur herstellung von meta-aromatischen polyamidfasern |
| US7683157B2 (en) | 2005-03-28 | 2010-03-23 | E.I. Du Pont De Nemours And Company | Process for the production of polyarenazole polymer |
-
2007
- 2007-12-18 EP EP07867802A patent/EP2111393A2/en not_active Withdrawn
- 2007-12-18 WO PCT/US2007/025816 patent/WO2008082509A2/en not_active Ceased
- 2007-12-18 KR KR1020097015149A patent/KR20090091348A/ko not_active Withdrawn
- 2007-12-18 US US12/519,592 patent/US8022167B2/en not_active Expired - Fee Related
- 2007-12-18 CN CNA2007800470753A patent/CN101563325A/zh active Pending
- 2007-12-18 JP JP2009542869A patent/JP2010513502A/ja not_active Abandoned
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