JP4739678B2 - モノハイドロペルフルオロアルカン、ビス（ペルフルオロアルキル）ホスフィン酸塩およびペルフルオロアルキルホスホン酸塩の合成方法 - Google Patents

モノハイドロペルフルオロアルカン、ビス（ペルフルオロアルキル）ホスフィン酸塩およびペルフルオロアルキルホスホン酸塩の合成方法 Download PDF

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JP4739678B2
JP4739678B2 JP2003584067A JP2003584067A JP4739678B2 JP 4739678 B2 JP4739678 B2 JP 4739678B2 JP 2003584067 A JP2003584067 A JP 2003584067A JP 2003584067 A JP2003584067 A JP 2003584067A JP 4739678 B2 JP4739678 B2 JP 4739678B2
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Prior art keywords
hydroxide
phosphorane
perfluoroalkyl
nmr
bis
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JP2005522511A (ja
JP2005522511A5 (enExample
Inventor
ニコライ イグナティフ，
ヴァイデン，ミヒャエル
ウルス ヴェルツ−ビーアマン，
ウド ハイダー，
ペーター ザルトリ，
アンドリー クチェリナ，
ヘルゲ ヴィルナー，
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Merck Patent GmbH
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Merck Patent GmbH
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Priority claimed from PCT/EP2003/002744 external-priority patent/WO2003087111A1/de
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Publication of JP2005522511A5 publication Critical patent/JP2005522511A5/ja
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
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    • B01J31/0287—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre
    • B01J31/0291—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre also containing elements or functional groups covered by B01J31/0201 - B01J31/0274
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    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
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    • B01J31/0231—Halogen-containing compounds
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    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
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    • B01J31/0278—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre
    • B01J31/0281—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member
    • B01J31/0284—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing nitrogen as cationic centre the nitrogen being a ring member of an aromatic ring, e.g. pyridinium
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B01J31/0277—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature
    • B01J31/0287—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides comprising ionic liquids, as components in catalyst systems or catalysts per se, the ionic liquid compounds being used in the molten state at the respective reaction temperature containing atoms other than nitrogen as cationic centre
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    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
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    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
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    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
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  • Engineering & Computer Science (AREA)
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  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
JP2003584067A 2002-04-16 2003-03-17 モノハイドロペルフルオロアルカン、ビス（ペルフルオロアルキル）ホスフィン酸塩およびペルフルオロアルキルホスホン酸塩の合成方法 Expired - Fee Related JP4739678B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
DE10216995.0 2002-04-16
DE10216995 2002-04-16
DE10220547A DE10220547A1 (de) 2002-04-16 2002-05-08 Verfahren zur Herstellung von Monohydro-Pefluoralkanen, Perfluoralkylphosphinaten und Perfluoralkylphosphonaten
DE10220547.7 2002-05-08
PCT/EP2003/002744 WO2003087111A1 (de) 2002-04-16 2003-03-17 Verfahren zur herstellung von monohydro-perfluoralkanen, bis(perfluoralkyl)phosphinaten und perfluoralkylphosphonaten

Publications (3)

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JP2005522511A JP2005522511A (ja) 2005-07-28
JP2005522511A5 JP2005522511A5 (enExample) 2006-05-11
JP4739678B2 true JP4739678B2 (ja) 2011-08-03

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JP2003584067A Expired - Fee Related JP4739678B2 (ja) 2002-04-16 2003-03-17 モノハイドロペルフルオロアルカン、ビス（ペルフルオロアルキル）ホスフィン酸塩およびペルフルオロアルキルホスホン酸塩の合成方法

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JP (1) JP4739678B2 (enExample)
KR (1) KR100937128B1 (enExample)
AT (1) ATE440102T1 (enExample)
DE (2) DE10220547A1 (enExample)
ES (1) ES2330427T3 (enExample)
TW (1) TWI328010B (enExample)
ZA (1) ZA200409161B (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10216997A1 (de) * 2002-04-16 2003-10-30 Merck Patent Gmbh Verfahren zur Herstellung von Bis(perfluoralkyl)phosphinsäuren und deren Salze
DE10353759A1 (de) * 2003-11-17 2005-06-16 Merck Patent Gmbh Verfahren zur Herstellung von Mono- und Bis/perfluoralkyl)phosphoranen und korrespondierenden Phosphaten
DE102006005579A1 (de) * 2006-02-06 2007-08-09 Cognis Ip Management Gmbh Verfahren zur Herstellung organischer Substanzen
FR2912748B1 (fr) * 2007-02-16 2009-11-13 Centre Nat Rech Scient Alkyl h-phosphonates de n,n'-dialkylimidazouliums, d'ammoniums quaternaires et leurs utilisations
DE102008035174A1 (de) * 2008-07-28 2010-02-11 Merck Patent Gmbh Verfahren zur Herstellung von Bis(fluoralkyl)-phosphinsäure oder Fluoralkylphosphonsäure
DE102009058969A1 (de) * 2009-12-18 2011-06-22 Merck Patent GmbH, 64293 Verbindung mit (Perfluoralkyl)fluorohydrogenphosphat - Anionen

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2233941C3 (de) * 1972-07-11 1978-03-02 Cassella Farbwerke Mainkur Ag, 6000 Frankfurt Verwendung von Perfluoralkylphosphorverbindungen als schaumdämpfende Mittel

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JP2005522511A (ja) 2005-07-28
TW200306980A (en) 2003-12-01
KR20040103965A (ko) 2004-12-09
ZA200409161B (en) 2005-05-31
DE10220547A1 (de) 2003-11-06
DE50311833D1 (de) 2009-10-01
ES2330427T3 (es) 2009-12-10
ATE440102T1 (de) 2009-09-15
TWI328010B (en) 2010-08-01
KR100937128B1 (ko) 2010-01-18

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