JP2011505421A5 - - Google Patents
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- Publication number
- JP2011505421A5 JP2011505421A5 JP2010537003A JP2010537003A JP2011505421A5 JP 2011505421 A5 JP2011505421 A5 JP 2011505421A5 JP 2010537003 A JP2010537003 A JP 2010537003A JP 2010537003 A JP2010537003 A JP 2010537003A JP 2011505421 A5 JP2011505421 A5 JP 2011505421A5
- Authority
- JP
- Japan
- Prior art keywords
- perfluoroalkyl
- optionally
- represented
- interrupted
- fluoroalkylamine
- 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
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 150000001408 amides Chemical class 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 125000001153 fluoro group Chemical group F* 0.000 claims description 6
- 125000000743 hydrocarbylene group Chemical group 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
- 125000000962 organic group Chemical group 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- -1 fluoroalkyl isocyanate Chemical class 0.000 claims description 5
- 150000002540 isothiocyanates Chemical class 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 2
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 claims description 2
- 239000007800 oxidant agent Substances 0.000 claims description 2
- 150000003573 thiols Chemical class 0.000 claims description 2
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000020176 deacylation Effects 0.000 description 1
- 238000005947 deacylation reaction Methods 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US524107P | 2007-12-03 | 2007-12-03 | |
| US61/005,241 | 2007-12-03 | ||
| US12/273,091 | 2008-11-18 | ||
| US12/273,091 US8153846B2 (en) | 2007-12-03 | 2008-11-18 | Sulfur containing fluoroalkyl amines and isocyanates |
| PCT/US2008/085100 WO2009073592A2 (en) | 2007-12-03 | 2008-12-01 | Sulfur containing fluoroalkyl amines and isocyanates |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011505421A JP2011505421A (ja) | 2011-02-24 |
| JP2011505421A5 true JP2011505421A5 (enExample) | 2011-12-22 |
| JP5497659B2 JP5497659B2 (ja) | 2014-05-21 |
Family
ID=40676434
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010537003A Expired - Fee Related JP5497659B2 (ja) | 2007-12-03 | 2008-12-01 | 硫黄含有フルオロアルキルアミンおよびイソシアナート |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8153846B2 (enExample) |
| EP (2) | EP2662354A2 (enExample) |
| JP (1) | JP5497659B2 (enExample) |
| KR (1) | KR20100101126A (enExample) |
| CN (1) | CN101939294A (enExample) |
| AU (1) | AU2008334034B2 (enExample) |
| CA (1) | CA2706610A1 (enExample) |
| NZ (1) | NZ585414A (enExample) |
| WO (1) | WO2009073592A2 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2483238B1 (en) * | 2009-09-28 | 2014-06-11 | Coatings Foreign IP Co. LLC | A coating composition comprising fluorinated sag control agent |
| SG194727A1 (en) * | 2011-05-13 | 2013-12-30 | Univ Nanyang Tech | Method for modification of organic molecules |
| FR3091870B1 (fr) * | 2019-01-18 | 2021-11-05 | Adisseo France Sas | Agent pour l’initiation d’une reaction d’addition radicalaire et procede le mettant en œuvre |
| JP2022532711A (ja) * | 2019-05-09 | 2022-07-19 | エンタープライズ ノーク インコーポレイテッド | 携帯型ファイヤピットおよびグリルアセンブリ |
| CN116836094A (zh) * | 2023-06-09 | 2023-10-03 | 福建三农新材料有限责任公司 | 一种全氟己基乙基硫醇的制备方法 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3655732A (en) | 1967-05-16 | 1972-04-11 | Du Pont | Fluorinated acrylic monomers containing hetero atoms and their polymers |
| NL6908449A (enExample) * | 1969-06-03 | 1970-12-07 | ||
| US4126633A (en) | 1973-09-12 | 1978-11-21 | Pennwalt Corporation | Fluorinated aliphatic sulfides |
| JPS5289633A (en) | 1976-01-17 | 1977-07-27 | Neos Kk | Perfluoroalkenyl aryl thioether derivatives |
| US4171282A (en) | 1977-12-07 | 1979-10-16 | Ciba-Geigy Corporation | Fluorinated nonionic surfactants |
| JPS57108063A (en) | 1980-12-26 | 1982-07-05 | Sagami Chem Res Center | Perfluoroalkylsulfinyl compound and its preparation |
| US4490304A (en) | 1982-12-29 | 1984-12-25 | Ciba-Geigy Corporation | Perfluoroalkyl thioalkylene amphoteric compounds |
| FR2592648B1 (fr) | 1986-01-07 | 1988-07-29 | Atochem | Composes polyfluoroalkylthio-methyliques, leurs procedes de preparation et leurs applications comme agents tensio-actifs ou precurseurs de ces derniers. |
| FR2609463B1 (fr) | 1987-01-13 | 1990-11-30 | Atochem | Synthese des perfluoroalkyl-2 ethanethiols |
| US5411766A (en) | 1989-12-29 | 1995-05-02 | E. I. Du Pont De Nemours And Company | Substrates treated with polyfluoro nitrogen containing organic compounds |
| DE4007048A1 (de) * | 1990-03-07 | 1991-09-12 | Hoechst Ag | N-acyl-aminoalkyl-2-hydroxyethylsulfide und ein verfahren zu ihrer herstellung |
| EP0600370B1 (de) * | 1992-12-02 | 1996-07-17 | Hoechst Aktiengesellschaft | Di-(3-(2-chlorethylsulfonyl)-l-propyl)-amin-Hydrochlorid und Verfahren zu seiner Herstellung |
| JP3572077B2 (ja) | 1993-07-29 | 2004-09-29 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | ヨウ化パーフルオロアルキル類の製造方法 |
| US5466877A (en) | 1994-03-15 | 1995-11-14 | Minnesota Mining And Manufacturing Company | Process for converting perfluorinated esters to perfluorinated acyl fluorides and/or ketones |
| US5728887A (en) | 1996-04-10 | 1998-03-17 | E. I. Du Pont De Nemours And Company | Catalytic hydrogenolysis of organic thiocyanates and disulfides to thiols |
| DE19807791A1 (de) | 1998-02-19 | 1999-08-26 | Schering Ag | Kombinationspräparat aus Östrogen und Antiöstrogen |
| DE10108543C1 (de) | 2001-02-22 | 2002-04-04 | Wacker Chemie Gmbh | Verfahren zur Herstellung von Isocyanatgruppen aufweisenden Organosiliciumverbindungen |
| DE10332197A1 (de) | 2003-07-15 | 2005-02-10 | Synthopol Chemie Dr.Rer.Pol. Koch Gmbh & Co Kg | Harze mit chemisch gekoppelten Perfluoralkylverbindung(en) und Verfahren zu ihrer Herstellung |
| DE10332152A1 (de) | 2003-07-15 | 2005-02-03 | Degussa Ag | (Poly-)Uretdione mit chemisch gekoppelten Perfluoralkylverbindungen und Verfahren zu ihrer Herstellung |
| DE10332198A1 (de) | 2003-07-15 | 2005-02-10 | Synthopol Chemie Dr.Rer.Pol. Koch Gmbh & Co Kg | Harze mit chemisch gekoppelten Perfluoralkansäureamid(en) und Verfahren zu ihrer Herstellung |
| US7470745B2 (en) | 2006-11-13 | 2008-12-30 | E. I. Du Pont De Nemours And Company | Perfluoroether based polymers |
-
2008
- 2008-11-18 US US12/273,091 patent/US8153846B2/en not_active Expired - Fee Related
- 2008-12-01 WO PCT/US2008/085100 patent/WO2009073592A2/en not_active Ceased
- 2008-12-01 EP EP13179255.8A patent/EP2662354A2/en not_active Withdrawn
- 2008-12-01 EP EP08857668.1A patent/EP2215056B1/en not_active Not-in-force
- 2008-12-01 CA CA2706610A patent/CA2706610A1/en not_active Abandoned
- 2008-12-01 AU AU2008334034A patent/AU2008334034B2/en not_active Ceased
- 2008-12-01 KR KR1020107014616A patent/KR20100101126A/ko not_active Withdrawn
- 2008-12-01 JP JP2010537003A patent/JP5497659B2/ja not_active Expired - Fee Related
- 2008-12-01 CN CN2008801190129A patent/CN101939294A/zh active Pending
- 2008-12-01 NZ NZ585414A patent/NZ585414A/en not_active IP Right Cessation
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