JP2009541429A5 - - Google Patents
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- JP2009541429A5 JP2009541429A5 JP2009517150A JP2009517150A JP2009541429A5 JP 2009541429 A5 JP2009541429 A5 JP 2009541429A5 JP 2009517150 A JP2009517150 A JP 2009517150A JP 2009517150 A JP2009517150 A JP 2009517150A JP 2009541429 A5 JP2009541429 A5 JP 2009541429A5
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- Prior art keywords
- formula
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- 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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- 150000001875 compounds Chemical class 0.000 claims 28
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 10
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims 8
- 239000003054 catalyst Substances 0.000 claims 7
- 239000002184 metal Substances 0.000 claims 7
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 5
- 238000005984 hydrogenation reaction Methods 0.000 claims 5
- -1 n-pentylaldehyde Chemical compound 0.000 claims 5
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 claims 5
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 claims 4
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 claims 4
- 150000001298 alcohols Chemical class 0.000 claims 2
- 150000001299 aldehydes Chemical class 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 claims 2
- 150000002432 hydroperoxides Chemical class 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 claims 1
- 125000003158 alcohol group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- RXFCIXRFAJRBSG-UHFFFAOYSA-N NCCCNCCNCCCN Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 2
- 0 CC(C)(CC(CC1(C)C)=O)N1O* Chemical compound CC(C)(CC(CC1(C)C)=O)N1O* 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06116619 | 2006-07-05 | ||
| EP07106899 | 2007-04-25 | ||
| PCT/EP2007/056301 WO2008003605A1 (en) | 2006-07-05 | 2007-06-25 | Process for the preparation of sterically hindered nitroxyl ethers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009541429A JP2009541429A (ja) | 2009-11-26 |
| JP2009541429A5 true JP2009541429A5 (enExample) | 2010-09-02 |
Family
ID=38894217
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009517150A Withdrawn JP2009541429A (ja) | 2006-07-05 | 2007-06-25 | 立体障害性ニトロキシルエーテルの製造方法 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US8481726B2 (enExample) |
| EP (1) | EP2035382B1 (enExample) |
| JP (1) | JP2009541429A (enExample) |
| KR (1) | KR101454702B1 (enExample) |
| AT (1) | ATE449072T1 (enExample) |
| CA (1) | CA2654837C (enExample) |
| DE (1) | DE602007003357D1 (enExample) |
| ES (1) | ES2335320T3 (enExample) |
| MX (1) | MX2009000047A (enExample) |
| TW (1) | TWI389887B (enExample) |
| WO (1) | WO2008003605A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011029744A1 (en) | 2009-09-10 | 2011-03-17 | Basf Se | Sterically hindered amine stabilizer |
| JP5777643B2 (ja) * | 2010-03-05 | 2015-09-09 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 立体障害アミン |
| WO2011107513A1 (en) | 2010-03-05 | 2011-09-09 | Basf Se | Sterically hindered amines |
| ES2541284T3 (es) | 2010-10-20 | 2015-07-17 | Basf Se | Fotoestabilizadores a base de aminas estéricamente impedidas con funcionalización mixta |
| JP5889315B2 (ja) | 2010-10-20 | 2016-03-22 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 特定の機能化を有するオリゴマー光安定剤 |
| CA2940970C (en) | 2014-02-28 | 2019-03-19 | Exxonmobil Chemical Patents Inc. | Mooney viscosity stable brominated elastomers |
| EP3288735B1 (en) | 2015-04-30 | 2024-07-03 | ExxonMobil Chemical Patents Inc. | Process for halogenating olefinic-derived elastomers in the bulk phase |
| CA3010059C (en) | 2016-01-29 | 2020-10-27 | Exxonmobil Chemical Patents Inc. | System and process for the production of functionalized olefinic-based polymer |
| CN112126060B (zh) | 2019-06-25 | 2022-05-31 | 北京天罡助剂有限责任公司 | 一种聚合型高分子空间位阻胺及其制备方法 |
| EP3996690B1 (en) | 2019-07-09 | 2023-08-02 | Basf Se | Tableting of specific polymer stabilizers |
| WO2021167096A1 (ja) | 2020-02-21 | 2021-08-26 | Ｐｓジャパン株式会社 | スチレン系樹脂組成物、難燃性スチレン系樹脂組成物及び成形体、並びにパッチアンテナ |
| CN112250668A (zh) * | 2020-10-10 | 2021-01-22 | 利安隆凯亚(河北)新材料有限公司 | N-烷氧基受阻胺光稳定剂及其中间体的制备方法 |
| CN113354813B (zh) * | 2021-06-02 | 2023-07-04 | 宿迁联盛科技股份有限公司 | 一种低碱性受阻胺光稳定剂nor 371的制备方法 |
| EP4504702A1 (en) | 2022-04-04 | 2025-02-12 | Zedda Innovation Consulting | Process for the preparation of sterically hindered nitroxyl ethers |
| WO2025067782A1 (en) | 2023-09-27 | 2025-04-03 | Geneuschem Ag | Preparation of n-alkoxyamine hals from corresponding hydroxylamines |
| CN118179610B (zh) * | 2024-05-16 | 2024-07-16 | 安徽海螺材料科技股份有限公司 | 一种合成环状碳酸酯用催化剂及其制备方法和应用 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4921962A (en) | 1988-10-19 | 1990-05-01 | Ciba-Geigy Corporation | Process for preparing N-hydrocarbyloxy derivatives of sterically hindered amines |
| US5374729A (en) * | 1992-05-07 | 1994-12-20 | Ciba-Geigy Corporation | Process for preparing N-methoxy derivatives of 4-hydroxy-2,2,6,6-tetramethylpiperidine and 2,2,6,6-tetramethyl-4-piperidone |
| GB0003326D0 (en) | 1999-02-25 | 2000-04-05 | Ciba Sc Holding Ag | Hydroxy-Substituted N-Alkoxy hindered amines |
| TW572896B (en) | 2000-05-26 | 2004-01-21 | Ciba Sc Holding Ag | Process for the synthesis of amine ethers from secondary amino oxides |
| TW200407307A (en) | 2001-11-26 | 2004-05-16 | Ciba Sc Holding Ag | Process for the synthesis of amine ethers from secondary amino oxides |
| MXPA06000522A (es) | 2003-07-14 | 2006-03-30 | Ciba Sc Holding Ag | Proceso catalizado con peroxido de hidrogeno para la preparacion de n-hidrocarbiloxiaminas estericamnte impedidas. |
| DE112005000536T5 (de) * | 2004-03-15 | 2007-02-01 | Ciba Specialty Chemicals Holding Inc. | Verfahren für die Synthese von Aminethern |
| ATE493387T1 (de) * | 2006-07-05 | 2011-01-15 | Basf Se | Verfahren zur herstellung sterisch gehinderter nitroxylether |
-
2007
- 2007-06-25 AT AT07786825T patent/ATE449072T1/de not_active IP Right Cessation
- 2007-06-25 KR KR1020087031543A patent/KR101454702B1/ko not_active Expired - Fee Related
- 2007-06-25 DE DE602007003357T patent/DE602007003357D1/de active Active
- 2007-06-25 MX MX2009000047A patent/MX2009000047A/es active IP Right Grant
- 2007-06-25 WO PCT/EP2007/056301 patent/WO2008003605A1/en not_active Ceased
- 2007-06-25 CA CA2654837A patent/CA2654837C/en not_active Expired - Fee Related
- 2007-06-25 US US12/308,595 patent/US8481726B2/en active Active
- 2007-06-25 JP JP2009517150A patent/JP2009541429A/ja not_active Withdrawn
- 2007-06-25 EP EP07786825A patent/EP2035382B1/en active Active
- 2007-06-25 ES ES07786825T patent/ES2335320T3/es active Active
- 2007-07-03 TW TW096124198A patent/TWI389887B/zh active