JP2005515258A5 - - Google Patents
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- JP2005515258A5 JP2005515258A5 JP2003562128A JP2003562128A JP2005515258A5 JP 2005515258 A5 JP2005515258 A5 JP 2005515258A5 JP 2003562128 A JP2003562128 A JP 2003562128A JP 2003562128 A JP2003562128 A JP 2003562128A JP 2005515258 A5 JP2005515258 A5 JP 2005515258A5
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- JP
- Japan
- Prior art keywords
- auxiliary base
- salt
- useful product
- liquid
- base
- 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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- 150000003839 salts Chemical class 0.000 claims 19
- 238000000034 method Methods 0.000 claims 15
- 239000007788 liquid Substances 0.000 claims 8
- 239000002253 acid Substances 0.000 claims 7
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 6
- -1 phosphite amide halide Chemical class 0.000 claims 5
- 239000002904 solvent Substances 0.000 claims 5
- 239000007791 liquid phase Substances 0.000 claims 4
- 238000000926 separation method Methods 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims 3
- 239000011541 reaction mixture Substances 0.000 claims 3
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 2
- 230000002378 acidificating effect Effects 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- SGUVLZREKBPKCE-UHFFFAOYSA-N 1,5-diazabicyclo[4.3.0]-non-5-ene Chemical compound C1CCN=C2CCCN21 SGUVLZREKBPKCE-UHFFFAOYSA-N 0.000 claims 1
- MCMFEZDRQOJKMN-UHFFFAOYSA-N 1-butylimidazole Chemical group CCCCN1C=CN=C1 MCMFEZDRQOJKMN-UHFFFAOYSA-N 0.000 claims 1
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 claims 1
- NRGGMCIBEHEAIL-UHFFFAOYSA-N 2-ethylpyridine Chemical compound CCC1=CC=CC=N1 NRGGMCIBEHEAIL-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- XQJHRCVXRAJIDY-UHFFFAOYSA-N aminophosphine Chemical compound PN XQJHRCVXRAJIDY-UHFFFAOYSA-N 0.000 claims 1
- OXJVPEPMGZHRJB-UHFFFAOYSA-N aminophosphinoamine Chemical compound NPN OXJVPEPMGZHRJB-UHFFFAOYSA-N 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 229910052799 carbon Chemical group 0.000 claims 1
- RLMOMHNXIWBGTF-UHFFFAOYSA-N diaminophosphinoamine Chemical compound NP(N)N RLMOMHNXIWBGTF-UHFFFAOYSA-N 0.000 claims 1
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- LEHULSCLOPRJSL-UHFFFAOYSA-N n,n-dibutylpentan-1-amine Chemical group CCCCCN(CCCC)CCCC LEHULSCLOPRJSL-UHFFFAOYSA-N 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 150000003018 phosphorus compounds Chemical class 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10202838A DE10202838A1 (de) | 2002-01-24 | 2002-01-24 | Verfahren zur Abtrennung von Säuren aus chemischen Reaktionsgemischen mit Hilfe von ionischen Flüssigkeiten |
| DE10202838.9 | 2002-01-24 | ||
| DE10230222.7 | 2002-07-04 | ||
| DE2002130222 DE10230222A1 (de) | 2002-07-04 | 2002-07-04 | Verfahren zur Abtrennung von Säuren aus chemischen Reaktionsgemischen mit Hilfe von Ionischen Flüssigkeiten |
| DE10248902.5 | 2002-10-18 | ||
| DE10248902A DE10248902A1 (de) | 2002-10-18 | 2002-10-18 | Verfahren zur Abtrennung von Säuren aus chemischen Reaktionsgemischen mit Hilfe von ionischen Flüssigkeiten |
| DE10251140A DE10251140A1 (de) | 2002-10-31 | 2002-10-31 | Verfahren zur Abtrennung von Säuren aus chemischen Reaktionsgemischen mit Hilfe von ionischen Flüssigkeiten |
| DE10251140.3 | 2002-10-31 | ||
| PCT/EP2003/000549 WO2003062251A1 (de) | 2002-01-24 | 2003-01-21 | Verfahren zur abtrennung von säuren aus chemischen reaktionsgemischen mit hilfe von ionischen flüssigkeiten |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005515258A JP2005515258A (ja) | 2005-05-26 |
| JP2005515258A5 true JP2005515258A5 (enExample) | 2006-01-05 |
| JP4939732B2 JP4939732B2 (ja) | 2012-05-30 |
Family
ID=27617633
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003562128A Expired - Fee Related JP4939732B2 (ja) | 2002-01-24 | 2003-01-21 | 化学反応混合物から酸をイオン性液体により分離する方法 |
| JP2003562056A Expired - Fee Related JP4950413B2 (ja) | 2002-01-24 | 2003-01-21 | 化学反応混合物から酸をイオン性液体により分離する方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003562056A Expired - Fee Related JP4950413B2 (ja) | 2002-01-24 | 2003-01-21 | 化学反応混合物から酸をイオン性液体により分離する方法 |
Country Status (17)
| Country | Link |
|---|---|
| US (3) | US7351339B2 (enExample) |
| EP (2) | EP1472201B1 (enExample) |
| JP (2) | JP4939732B2 (enExample) |
| KR (2) | KR100891629B1 (enExample) |
| CN (2) | CN100349833C (enExample) |
| AR (1) | AR038161A1 (enExample) |
| AT (1) | ATE358134T1 (enExample) |
| BR (1) | BR0306886B1 (enExample) |
| CA (2) | CA2473954C (enExample) |
| DE (1) | DE50306900D1 (enExample) |
| ES (2) | ES2515791T3 (enExample) |
| MX (1) | MXPA04006695A (enExample) |
| MY (1) | MY138064A (enExample) |
| NO (1) | NO330257B1 (enExample) |
| SA (1) | SA03230520B1 (enExample) |
| TW (1) | TWI325862B (enExample) |
| WO (2) | WO2003062251A1 (enExample) |
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| KR100851101B1 (ko) * | 2001-03-29 | 2008-08-08 | 바스프 에스이 | Ｖｉｉｉ 아족 금속과의 니코겐 킬레이트 착물용 리간드및 히드로포르밀화, 카르보닐화, 히드로시안화 또는수소화 반응을 위한 촉매로서의 착물의 용도 |
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| DE10350999A1 (de) | 2003-10-30 | 2005-06-02 | Basf Ag | Katalysator, umfassend wenigstens einen Nickel(O)Komplex stabilisiert durch einen sterisch anspruchsvollen Chelatphosphinitphosphitliganden, sowie ein Verfahren zur Herstellung von Nitrilen |
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-
2003
- 2003-01-17 MY MYPI20030151A patent/MY138064A/en unknown
- 2003-01-17 AR ARP030100139A patent/AR038161A1/es active IP Right Grant
- 2003-01-21 US US10/467,065 patent/US7351339B2/en not_active Expired - Lifetime
- 2003-01-21 ES ES03702479.1T patent/ES2515791T3/es not_active Expired - Lifetime
- 2003-01-21 CN CNB038027399A patent/CN100349833C/zh not_active Expired - Fee Related
- 2003-01-21 DE DE50306900T patent/DE50306900D1/de not_active Expired - Lifetime
- 2003-01-21 ES ES03704443T patent/ES2283749T3/es not_active Expired - Lifetime
- 2003-01-21 CA CA2473954A patent/CA2473954C/en not_active Expired - Fee Related
- 2003-01-21 EP EP03702479.1A patent/EP1472201B1/de not_active Expired - Lifetime
- 2003-01-21 US US10/500,145 patent/US7767852B2/en not_active Expired - Fee Related
- 2003-01-21 EP EP03704443A patent/EP1470136B1/de not_active Expired - Lifetime
- 2003-01-21 JP JP2003562128A patent/JP4939732B2/ja not_active Expired - Fee Related
- 2003-01-21 AT AT03704443T patent/ATE358134T1/de not_active IP Right Cessation
- 2003-01-21 KR KR1020047011396A patent/KR100891629B1/ko not_active Expired - Fee Related
- 2003-01-21 JP JP2003562056A patent/JP4950413B2/ja not_active Expired - Fee Related
- 2003-01-21 KR KR1020047011490A patent/KR100891140B1/ko not_active Expired - Fee Related
- 2003-01-21 WO PCT/EP2003/000549 patent/WO2003062251A1/de not_active Ceased
- 2003-01-21 MX MXPA04006695A patent/MXPA04006695A/es active IP Right Grant
- 2003-01-21 CN CNB038027429A patent/CN1300156C/zh not_active Expired - Fee Related
- 2003-01-21 WO PCT/EP2003/000545 patent/WO2003062171A2/de not_active Ceased
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- 2003-01-21 BR BRPI0306886-2A patent/BR0306886B1/pt not_active IP Right Cessation
- 2003-01-22 SA SA03230520A patent/SA03230520B1/ar unknown
- 2003-01-24 TW TW092101588A patent/TWI325862B/zh not_active IP Right Cessation
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2004
- 2004-08-23 NO NO20043512A patent/NO330257B1/no not_active IP Right Cessation
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- 2007-12-07 US US11/952,242 patent/US20080083606A1/en not_active Abandoned
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