JP2004534778A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2004534778A5 JP2004534778A5 JP2003500042A JP2003500042A JP2004534778A5 JP 2004534778 A5 JP2004534778 A5 JP 2004534778A5 JP 2003500042 A JP2003500042 A JP 2003500042A JP 2003500042 A JP2003500042 A JP 2003500042A JP 2004534778 A5 JP2004534778 A5 JP 2004534778A5
- Authority
- JP
- Japan
- Prior art keywords
- hydroxide
- quaternary ammonium
- modifier
- dinitrile
- quaternary
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 claims 16
- 125000001453 quaternary ammonium group Chemical group 0.000 claims 14
- 239000003607 modifier Substances 0.000 claims 11
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical group [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 claims 8
- 239000003054 catalyst Substances 0.000 claims 6
- 239000000908 ammonium hydroxide Substances 0.000 claims 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 4
- 125000005219 aminonitrile group Chemical group 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 150000004985 diamines Chemical class 0.000 claims 4
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 claims 4
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 3
- 239000011541 reaction mixture Substances 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 229910021472 group 8 element Inorganic materials 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 2
- 229910052759 nickel Inorganic materials 0.000 claims 2
- 125000005496 phosphonium group Chemical group 0.000 claims 2
- 238000002407 reforming Methods 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- DFQPZDGUFQJANM-UHFFFAOYSA-M tetrabutylphosphanium;hydroxide Chemical compound [OH-].CCCC[P+](CCCC)(CCCC)CCCC DFQPZDGUFQJANM-UHFFFAOYSA-M 0.000 claims 2
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 claims 2
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 claims 2
- LPSKDVINWQNWFE-UHFFFAOYSA-M tetrapropylazanium;hydroxide Chemical compound [OH-].CCC[N+](CCC)(CCC)CCC LPSKDVINWQNWFE-UHFFFAOYSA-M 0.000 claims 2
- 230000036571 hydration Effects 0.000 claims 1
- 238000006703 hydration reaction Methods 0.000 claims 1
- DJFBJKSMACBYBD-UHFFFAOYSA-N phosphane;hydrate Chemical group O.P DJFBJKSMACBYBD-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/871,102 US6376714B1 (en) | 2001-05-31 | 2001-05-31 | Environmentally friendly process for the hydrogenation of dinitriles |
| PCT/US2002/016374 WO2002096862A2 (en) | 2001-05-31 | 2002-05-24 | Environmentally friendly process for the hydrogenation of dinitriles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2004534778A JP2004534778A (ja) | 2004-11-18 |
| JP2004534778A5 true JP2004534778A5 (enExample) | 2005-12-22 |
Family
ID=25356731
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003500042A Withdrawn JP2004534778A (ja) | 2001-05-31 | 2002-05-24 | ジニトリルの環境調和型水素化プロセス |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6376714B1 (enExample) |
| EP (1) | EP1392646A2 (enExample) |
| JP (1) | JP2004534778A (enExample) |
| KR (1) | KR20040004667A (enExample) |
| CN (1) | CN1531523A (enExample) |
| BR (1) | BR0210082A (enExample) |
| CA (1) | CA2444442A1 (enExample) |
| MX (1) | MXPA03010927A (enExample) |
| MY (1) | MY134178A (enExample) |
| PL (1) | PL364602A1 (enExample) |
| RU (1) | RU2003137530A (enExample) |
| SK (1) | SK14492003A3 (enExample) |
| TW (1) | TW593235B (enExample) |
| WO (1) | WO2002096862A2 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6569802B1 (en) * | 1999-11-30 | 2003-05-27 | E. I. Du Pont De Nemours And Company | Catalyst for selective hydrogenation of dinitriles |
| US7132562B2 (en) | 2003-11-12 | 2006-11-07 | Invista North America S.A R.L. | Use of modifiers in a dinitrile hydrogenation process |
| DE10361071A1 (de) * | 2003-12-22 | 2005-07-14 | Basf Ag | Nitrilhydrierung in Gegenwart Ionischer Flüssigkeiten |
| JP2008522969A (ja) * | 2004-12-07 | 2008-07-03 | インヴィスタ テクノロジー エスアエルエル | ジニトリル水素化方法における調節剤の使用 |
| DE102006061533A1 (de) * | 2006-12-27 | 2008-07-03 | Saltigo Gmbh | Verfahren zur Herstellung von 2-Aminomethylpiperidin |
| JP2013528603A (ja) * | 2010-05-19 | 2013-07-11 | ビオアンブ,ソシエテ パ アクシオンス シンプリフィエ | ジアミノブタン(dab)、コハク酸ジニトリル(sdn)及びスクシンアミド(dam)を生産する方法 |
| JP2013531624A (ja) * | 2010-05-19 | 2013-08-08 | ビオアンブ,ソシエテ パ アクシオンス シンプリフィエ | ジアミノブタン(dab)、コハク酸ジニトリル(sdn)及びスクシンアミド(dam)を生産する方法 |
| WO2011159557A1 (en) | 2010-06-16 | 2011-12-22 | Bioamber S.A.S. | Processes for producing hexamethylenediamine (hmd), adiponitrile (adn), adipamide (adm) and derivatives thereof |
| JP2013533863A (ja) | 2010-06-16 | 2013-08-29 | ビオアンブ,ソシエテ パ アクシオンス シンプリフィエ | ヘキサメチレンジアミン(hmd)、アジポニトリル(adn)、アジパミド(adm)及びそれらの誘導体の製造方法 |
| WO2012158182A1 (en) | 2011-05-17 | 2012-11-22 | Bioamber S.A.S. | Processes for producing butanediol and diaminobutane from fermentation broths containing ammonium succinates |
| US9464030B2 (en) | 2011-05-18 | 2016-10-11 | Bioamber Inc. | Processes for producing butanediol (BDO), diaminobutane (DAB), succinic dinitrile (SDN) and succinamide (DAM) |
| WO2012170060A1 (en) | 2011-06-10 | 2012-12-13 | Bioamber S.A.S. | Processes for producing hexanediol (hdo), hexamethylenediamine (hmd), and derivatives thereof |
| WO2013149373A1 (zh) * | 2012-04-01 | 2013-10-10 | 烟台万华聚氨酯股份有限公司 | 一种n-(2-氨乙基)-1,2-乙二胺的制备方法 |
| CN105555752A (zh) | 2013-09-13 | 2016-05-04 | 因温斯特技术公司 | 使二腈氢化以便制备二胺 |
| CN105658617A (zh) | 2013-09-13 | 2016-06-08 | 因温斯特技术公司 | 使二腈氢化以便制备二胺 |
| WO2015038679A1 (en) | 2013-09-13 | 2015-03-19 | Invista Technologies S.A R.L. | Catalyst preparation and hydrogenation process |
| WO2015038675A1 (en) | 2013-09-13 | 2015-03-19 | Invista Technologies S.À R.L. | Hydrogenation process for making diamine from dinitrile |
| CN105555753A (zh) | 2013-09-13 | 2016-05-04 | 因温斯特技术公司 | 从二腈制备二胺的氢化方法 |
| CN106536476B (zh) | 2014-04-25 | 2018-11-13 | 英威达纺织(英国)有限公司 | 通过使二腈氢化来制备二胺 |
| WO2015200630A1 (en) | 2014-06-27 | 2015-12-30 | Invista North America S.A R.L. | Integrated process for nitrile manufacture with enhanced liquid-liquid extraction |
| WO2017142898A1 (en) | 2016-02-16 | 2017-08-24 | Invista North America S.A R.L. | Promoter for selective nitrile hydrogenation |
| EP4126812B1 (en) * | 2020-03-25 | 2025-11-05 | Basf Se | Process for the preparation of hexamethylenediamine by hydrogenation of adiponitrile in the presence of raney nickel and a basic co-catalyst |
| CN116535321A (zh) * | 2022-01-29 | 2023-08-04 | 北京旭阳科技有限公司 | 壬二腈加氢制备壬二胺的方法 |
| CN117603161A (zh) * | 2023-11-28 | 2024-02-27 | 万华化学集团股份有限公司 | 一种环己亚胺季铵碱、己二腈加氢制备己二胺的方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE700877A (enExample) * | 1966-07-04 | 1967-12-18 | ||
| US3773832A (en) * | 1970-01-16 | 1973-11-20 | Du Pont | Hydrogenation of adiponitrile over alkali-modified cobalt catalyst |
| US4721811A (en) | 1985-08-26 | 1988-01-26 | W. R. Grace & Co. | Synthesis of aliphatic polyamines |
| US5900511A (en) | 1997-03-28 | 1999-05-04 | E. I. De Pont De Nemours And Company | Process for continuous hydrogenation of adiponitrile |
| JP2002543057A (ja) * | 1999-04-28 | 2002-12-17 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | アミノニトリルの生成 |
| US6309758B1 (en) | 1999-05-06 | 2001-10-30 | W. R. Grace & Co.-Conn. | Promoted porous catalyst |
-
2001
- 2001-05-31 US US09/871,102 patent/US6376714B1/en not_active Expired - Lifetime
-
2002
- 2002-05-17 TW TW091110365A patent/TW593235B/zh not_active IP Right Cessation
- 2002-05-24 SK SK1449-2003A patent/SK14492003A3/sk not_active Application Discontinuation
- 2002-05-24 MX MXPA03010927A patent/MXPA03010927A/es unknown
- 2002-05-24 BR BR0210082-7A patent/BR0210082A/pt not_active IP Right Cessation
- 2002-05-24 EP EP02739372A patent/EP1392646A2/en not_active Withdrawn
- 2002-05-24 WO PCT/US2002/016374 patent/WO2002096862A2/en not_active Ceased
- 2002-05-24 JP JP2003500042A patent/JP2004534778A/ja not_active Withdrawn
- 2002-05-24 CN CNA028109155A patent/CN1531523A/zh active Pending
- 2002-05-24 CA CA002444442A patent/CA2444442A1/en not_active Abandoned
- 2002-05-24 KR KR20037015547A patent/KR20040004667A/ko not_active Withdrawn
- 2002-05-24 RU RU2003137530/04A patent/RU2003137530A/ru not_active Application Discontinuation
- 2002-05-24 PL PL02364602A patent/PL364602A1/xx unknown
- 2002-05-28 MY MYPI20021949A patent/MY134178A/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2004534778A5 (enExample) | ||
| RU2003137530A (ru) | Дружественный к окружающей среде способ гидрирования динитрилов | |
| EP1454880A4 (en) | METHOD FOR PRODUCING FUNCTIONAL NANOMATERIALS BY USING A ENDOTHERIC REACTION | |
| JP2005500399A (ja) | エフェドリンなどのアミン及び中間体の合成方法 | |
| JP2008296066A (ja) | 環状炭酸エステルの合成のための固定化触媒に用いる触媒架橋剤の製造方法、及びその固定化触媒の製造方法、及びその固定化触媒に用いる触媒架橋剤、及びその固定化触媒 | |
| JP2007502353A5 (enExample) | ||
| CN1754866A (zh) | 一种催化氧化苯乙烯的方法 | |
| WO2003101939A3 (en) | Method for the preparation of halogenated benzonitriles | |
| JP5380051B2 (ja) | 1,3−ジアルキル−2−イミダゾリジノン類の製造方法 | |
| CN111790452B (zh) | 一种甲醇羰基化催化剂及其制备方法、应用 | |
| TW200950884A (en) | (N-heterocyclic carbene) copper salt complex as latent click catalyst | |
| TW200710095A (en) | Process for producing organoalkoxysilanes from organic acids or cyanates and haloalkylalkoxysilanes | |
| CN1638866A (zh) | 改进具有mww结构的结晶硅钛酸盐催化剂的方法 | |
| WO2014067242A1 (zh) | 一种n1-(2-氨乙基)-1,2-乙二胺的制备方法 | |
| US6689913B2 (en) | Process for preparing terbinafine and HCI salt thereof | |
| JP2004067684A5 (enExample) | ||
| JP2011518822A (ja) | 新規な1,4−ジシラシクロヘキサン誘導体及びその製造方法 | |
| Nitta | Asymmetric Hydrogenation of α, β-Unsaturated Carboxylic Acids withModified Palladium Catalysts | |
| CN101068775B (zh) | 改性剂在二腈氢化方法中的应用 | |
| CN107840857A (zh) | 一种硼氢化物催化酮的硅腈化反应方法 | |
| CN1284767C (zh) | 甲基乙基酮连氮的合成方法 | |
| JP2005139182A5 (enExample) | ||
| CN103130749A (zh) | 一种环己烯氧化制备环氧环己烷的方法 | |
| CN1152858C (zh) | 联产环内酰胺与环胺的方法 | |
| CN107954835A (zh) | 一种制备二氯丙醇的方法 |