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US4810480A Expired / Lapsed US ⏱️ 0.0 years remaining

Preparation of polychlorophosphazene

Assignee: Arkema France SA
•
Filing: 1988-03-10
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Granted: 1989-03-07
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Expires: 2008-03-10
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Abstract

Abstract Polychlorophosphazene [Cl 2 (O)P[NPCl 2 ] n Cl] is more rapidly produced by polycondensing N-(dichlorophosphoryl)-trichlorophosphazene [P 2 NOCl 5 ] in the presence of a catalytically effective amount of a tertiary amine.

Inventors

  • 👤 Jean-Paul Chambrette
  • 👤 Roger De Jaeger
  • 👤 Philippe Potin

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 16:42
CPC Classifications
C; C01; C01B; C01B21/00; C01B21/082; C01B21/097; C01B21/098; C01B21/0986; C01B25/00; C01B25/10

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 45 words
A process for the preparation of polychlorophosphazene [Cl 2 (O)P[NPCl 2 ] n Cl], comprising polycondensing N-(dichlorophosphoryl)trichlorophosphazene [P 2 NOCl 5 ], at least a part of the polycondensation reaction being carried out in the presence of a catalytically effective amount of a tertiary amine.
Claim 2
Dependent Claim 45 words
A process for the preparation of polychlorophosphazene [Cl 2 (O)P[NPCl 2 ] n Cl], comprising polycondensing N-(dichlorophosphoryl)trichlorophosphazene [P 2 NOCl 5 ], at least a part of the polycondensation reaction being carried out in the presence of a catalytically effective amount of a tertiary amine.
Claim 3
Dependent Claim 95 words
The process as defined by claim 1, said teritary amine comprising an aliphatic amine containing at least twelve carbon atoms, a mono- or polycyclic aromatic amine, the aromatic nuclei of which being optionally substituted with halogen atoms or alkyl radicals containing up to 3 carbon atoms, heterocyclic amines containing 1 or 2 nitrogen atoms and, optionally, other heteroatoms, substituted such heterocycles bearing at least one halogen atom or alkyl radical substituent containing up to 3 carbon atoms, aralkyl or aryl groups, or forming, together with one or more aromatic ring members, a condensed polycyclic system.
Claim 4
Dependent Claim 40 words
The process as defined by claim 1, said tertiary amine comprising tributylamine; triisopentylamine; tripentylamine; trihexylamine; tris(2-methylbutyl)amine; triheptylamine; trioctylamine; tridecylamine; triphenylamine; N,N-dimethyl-α-naphthylamine; N,N-dimethyl-β-naphthylamine; 2,6-dibromopyridine; 2-phenyl, 3-phenyl and 4-phenylpyridines; 2,3,4-trimethyl, 2,3,5-trimethyl, 2,3,6-trimethyl, 2,4,5-trimethyl or 2,4,6-trimethylpyridine; 4-butylmorpholine; 4-benzylmorpholine; 4-phenylmorpholine; benzothiazole; phenanthridine; or 2,4-dichloro-5-methylpyrimidine.
Claim 5
Dependent Claim 14 words
The process as defined by claim 2, said tertiary amine comprising a substituted pyridine.
Claim 6
Dependent Claim 18 words
The process as defined by claim 1, said tertiary amine being stable at a temperature of 200° C.
Claim 7
Dependent Claim 18 words
The process as defined by claim 1, said tertiary amine being stable at a temperature of 240° C.
Claim 8
Dependent Claim 23 words
The process as defined by claim 1, carried out in the presence of from 0.2 to 1.5 mole % of the tertiary amine.
Claim 9
Dependent Claim 14 words
The process as defined by claim 1, carried out in an aromatic solvent medium.
Claim 10
Dependent Claim 13 words
The process as defined by claim 1, said tertiary amine comprising a trimethylpyridine.

References Cited (Backward Citations)

US2975028A Cited
US2925320A Cited
US4377558A Cited
US4544536A Cited
US4693876A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1992-03-06 1992-09-05 1993-03-07 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1996-03-06 1996-09-05 1997-03-07 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2000-03-06 2000-09-05 2001-03-07 $7700.00 Window Closed / Lapsed

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