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US4329458A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the preparation of 2,4,6-trifluoro-1,3,5-triazine

Assignee: Bayer AG
•
Filing: 1981-02-26
•
Granted: 1982-05-11
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Expires: 2001-02-26
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Abstract

Abstract The present invention relates to a process for the preparation of 2,4,6-trifluoro-1,3,5-triazine (TFT) from 2,4,6-trichloro-1,3,5-triazine (TCT) or from mixed chlorinated/fluorinated 1,3,5-triazines by fluorination with sodium fluoride in dipolar aprotic solvents. The process is characterized in that TCT or mixed chlorinated/fluorinated 1,3,5-triazines or mixtures thereof are metered into a suspension of sodium fluoride in a dipolar, aprotic solvent, which is warmed to a temperature of between 120° C. and 220° C. and optionally contains a further solvent.

Inventors

  • 👤 Erich Klauke
  • 👤 Ernst Kysela
  • 👤 Arnd Stuwe
  • 👤 Alfons Dorlars

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 16:26
CPC Classifications
C; C07; C07D; C07D251/00; C07D251/02; C07D251/12; C07D251/26; C07D251/28

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 53 words
Process for the preparation of 2,4,6-trifluoro-1,3,5-triazine (TFT) from 2,4,6-trichloro-1,3,5-triazine (TCT) or from mixed chlorinated/fluorinated 1,3,5-triazines by fluorination with NaF in a dipolar, aprotic solvent, characterised in that TCT is metered into a suspension warmed to 120° C. to 220° C., of NaF in a dipolar, aprotic solvent, which optionally contains a further solvent.
Claim 2
Dependent Claim 53 words
Process for the preparation of 2,4,6-trifluoro-1,3,5-triazine (TFT) from 2,4,6-trichloro-1,3,5-triazine (TCT) or from mixed chlorinated/fluorinated 1,3,5-triazines by fluorination with NaF in a dipolar, aprotic solvent, characterised in that TCT is metered into a suspension warmed to 120° C. to 220° C., of NaF in a dipolar, aprotic solvent, which optionally contains a further solvent.
Claim 3
Dependent Claim 14 words
Process according to claim 1, characterised in that the dipolar, aprotic solvent is tetramethylenesulphone.
Claim 4
Dependent Claim 42 words
Process according to claim 1, characterised in that a further solvent which is inert and which has a boiling point between the boiling point of TFT and the boiling point of the dipolar, aprotic solvent is added to the dipolar, aprotic solvent.
Claim 5
Dependent Claim 36 words
Process according to claim 1, characterised in that TCT is employed as a melt or as a solution or suspension in one of the solvents employed in the reaction or in a mixture of these solvents.
Claim 6
Dependent Claim 28 words
Process according to claim 1, characterised in that TCT is metered in as a mixture with or solution in mixed chlorinated/fluorinated 1,3,5-triazines, or mixed chlorinated/fluorinated 1,3,5-triazines are used.
Claim 7
Dependent Claim 29 words
Process according to claim 1, characterised in that the further solvents used are preferably those which have boiling points between 120°-200° C. and which are halogenated hydrocarbons or alkylbenzenes.
Claim 8
Dependent Claim 31 words
Process according to claim 6, characterised in that the halogenated hydrocarbon employed as the further solvent is chlorobenzene or 1,2-dichlorobenzene and the alkylbenzenes are o-, m- or p-xylene, or mixtures thereof.
Claim 9
Dependent Claim 26 words
Process according to claim 3, characterised in that the second solvent is employed in an amount of 0.05-0.6 mol, relative to the dipolar, aprotic solvent employed.

References Cited (Backward Citations)

US3008798A Cited
US3641020A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-05-10 1985-11-09 1986-05-11 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-05-10 1989-11-09 1990-05-11 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-05-10 1993-11-09 1994-05-11 $7700.00 Window Closed / Lapsed

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