Organic compounds -- part of the class 532-570 series – Organic compounds – Halogen containing
Reexamination Certificate
1998-09-14
2003-09-02
Barts, Samuel (Department: 1621)
Organic compounds -- part of the class 532-570 series
Organic compounds
Halogen containing
C570S144000
Reexamination Certificate
active
06613948
ABSTRACT:
The present invention relates to an improved process for the preparation of 2,3,4,5-tetrafluorobenzene derivatives from 2,3,4,5-tetrachloro- and/or 2,3,4.5-tetra-(chloro, fluoro)-benzene derivatives by chlorine/fluorine exchange.
DE-A 3 420 796 describes a process for the preparation of 2,3,4,5-tetrafluorobenzene derivatives, in which 2,3,4,5-tetrachlorobenzene derivatives are reacted with potassium fluoride in a solvent at elevated temperature. Using 2,3,4,5-tetrachlorobenzoyl fluoride as starting material and continuously distilling off the mixture of the fluorination products at from 800 to 500 mbar produces, after fractional distillation of the mixture of the fluorination products, the desired 2,3,4,5-tetrafluorobenzoyl fluoride in a yield of only 10% of theory, while significantly more undesired fluorination products are obtained, namely 2,3,4-trifluoro-5-chlorobenzoyl fluoride in a yield of 43% of theory and 2,4-difluoro-3,5-dichlorobenzoyl fluoride in a yield of 14% of theory (see Example 2 in DE-A). If 2,3,4,5-tetrachlorobenzonitrile is used as starting material and the fluorination mixture is subjected to fractional distillation, the ratios are obviously similar, although no information concerning the amounts of the tetrafluoro-, tetrafluorochloro- and difluorodichlorobenzonitriles obtained is given (see Example 5 in DE-A).
EP-A 607 824 describes a process for the preparation of 2,3,4,5-tetrafluoro-benzotrifluoride by reacting tetrachlorobenzotrifluoride with potassium fluoride. Using pure 2,3,4,5-tetrachlorobenzotrifluoride as starting material and working up the reaction mixture by distillation gives a crude distillate which comprises the 2,3,4,5-tetrafluorobenizotifluoride in an amount of from 54 to 62% of theory (see Example Group A. 4th example, parts a), b), c) and e) in EP-A). If mixtures of 2,3,4,5-tetrachloro- and 2,3,4-trifluoro-5-chlorobenzotrilfluoide are used as starting materials, the content of 2,3,4,5-tetrafluorobenizotifluoride in the crude distillate drops to 51% of theory (see Example group A. 4th example, part d) in EP-A). For recovery rates (i.e. the sum of the yields of 2,3,4,5-tetrafluoro- and 2,3,4-trifluoro-5-chlorobenzotrilfluoide) of about 90%, the yields of 2,3,4,5-tetrafluoro-benzo-trifluoride are only from 50 to 55% of theory, but the yields of 2,3,4-trifluoro-5-chlorobenzotrifluoride are from 34 to 38% of theory (see Example Group A, 4th Example, parts d) and e) in EP-A). This means that in order to prepare 2,3,4,5-tetrafluorobenzotrifluoride, from almost 40 to 50% of the recovery rate of 2,3,4-trifluoro-5-chlorobenzotrifluoride must be recycled, and thus the expenditure is high and the space-time yield is low.
There therefore continues to be a need for a process for the preparation of 2,3,4,5-tetrafluorobenzene derivatives in which the desired products are obtained in good yields and selectivities.
We have now found a process for the preparation of tetrafluorobenzene derivatives of the formula (I)
in which
R is CF
3
, CN or COF.
by reacting a chlorobenzene derivative of the formula
in which
R is as defined for formula (I), and
X
1
, X
2
and X
3
independently of one another are each F or Cl,
with a fluorinating agent in the presence of a solvent and a catalyst at elevated temperature, which comprises carrying out the reaction initially under temperature and pressure conditions such that the respective compound of the formula (I) is continuously distilled off through a column, and subsequently setting the temperature and pressure conditions such that remaining fractions of the compound of the formula (I) are distilled off together with the corresponding 2,3,4-trifluoro-5-chloro compound.
The novel process preferably uses compounds of the formula (II) in which X
1
, X
2
and X
3
are chlorine or those compounds of the formula (II) in a mixture with compounds of the formula (II) in which X
1
, X
2
and X
3
are fluorine.
Examples of suitable fluorinating agents are alkali metal fluorides, such as sodium fluoride, potassium fluoride, cesium fluoride and mixtures of said fluorides. Preference is given to potassium fluoride, particularly in spray-dried form.
Per equivalent of chlorine atoms to be replaced, it is possible to use, for example, at least 1 equivalent of fluorinatin agent. This amount is preferably from 1.1 to 1.5 equivalents of fluorinating agent. Larger amounts do not cause any problems, but are uneconomical.
Suitable solvents are dipolar aprotic solvents, such as tetramethylene sulfone (sulfolane). N-methylpyrrolidone, dimethyl sulfoxide, dimethylformanide, dimethyl-acetamide, diglyme, tetraglyme and 1,3-dimethyliymiidalzolidinonc. Preference is given to tetramethylene Sulfone (sulfolane). The solvent can be used, for example, in an amount of from 1 kg to 10 kg, based on 1 kg of fluorinating reagent. Larger amounts do not cause any problems, but are uneconomical.
Examples of suitable catalysts are phase transfer catalysts, such as quaternary ammonium salts, pyridinium salts, quaternary phosphonium salts and crown ethers. Individual examples which may be mentioned are: tetramethylammonium chloride, tetrabutylammonium bromide, N-neopentyl-4-(N′,N′-dimethylamino)-pyridinium chloride, tetrabutylphosphonium bromide, tetraphenylphosphonium bromide and 18-crown 6. Preference is given to tetraphenylphosphonium bromide. Based on the starting compound(s) of the formula (II), from 1 to 50% by weight, preferably from 4 to 15% by weight, of catalyst, based on the feed material, may, for example, be used.
The reaction temperature can be, for example, in the range from 160 to 250° C., it is preferably in the range from 190 to 230° C.
It is an essential feature of the present invention that, for a given reaction temperature, the pressure is initially set such that the respective compound of the formula (I) is continuously distilled off. The optimum pressure in each individual case can be easily determined by routine preliminary tests. It has been found that pressures in the range from, for example, 1.3 to 6 bar, frequently in the range from 2 to 4 bar, are generally required for this purpose.
The compound of the formula (I) produced during the reaction is generally the lowest boiling component of the reaction mixture. The pressure is initially chosen such that practically only the compound of the formula (I) formed distills off and practically none of the higher boiling constituents of the reaction mixture. When tetrachlorobenzotrifluoride and a reaction temperature of from 200 to 220° C. are used, pressures in the range from 2.1 to 2.3 bar, for example, have proven successful.
After the reaction has ended, virtually no more of compound of the formula (I) passes over and the pressure drops. From this moment, pressure and temperature conditions are set according to the invention such that fractions of the compound of the formula (I) still present in the reaction mixture distill of together with the corresponding 2,3,4-trifluoro-5-chloro compound. To achieve this, it is generally sufficient to only lower the pressure, for example, down to a rank from 50 to 200 mbar. It is preferable to collect the first fraction (=virtually pure compound of the formula (I)) and the second fraction (=mixture of the compound of the formula (I) and the corresponding 2,3,4-trifluoro-5-chloro compound) separately from one another.
The whole of the second fraction, or, in an advantageous manner, only the partially fluorinated compounds present therein after they have been removed, is/are added to the next batch in order to carry out the novel reaction to give the compound of the formula (I).
Compounds of the formula (I) are obtained in the novel way in significantly better yields and selectivities than previously. In the case of the novel process, the yields of compounds of the formula (I) are, for example, in the range from 65 to 75% of theory and the yields of corresponding 2,3,4-trifluoro-5-chloro compounds are, for example, in the range from only 12 to 18% of theory. This means that, in a straight pass, significantly more of the produ
Bielefeldt Dietmar
Holzbrecher Michael
Lui Norbert
Neuner Otto
Barts Samuel
Bayer AG
Brinks Hofer Gilson & Lione
Price Elvis O.
Zayia Gregory H.
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