WO2001096266A1 - Processes for fluorinating aromatic ring compounds - Google Patents

Processes for fluorinating aromatic ring compounds Download PDF

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Publication number
WO2001096266A1
WO2001096266A1 PCT/US2000/016127 US0016127W WO0196266A1 WO 2001096266 A1 WO2001096266 A1 WO 2001096266A1 US 0016127 W US0016127 W US 0016127W WO 0196266 A1 WO0196266 A1 WO 0196266A1
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Prior art keywords
fluoride
metal fluoride
composition
cupric
benzene
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Ceased
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PCT/US2000/016127
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French (fr)
Inventor
Munirpallam A. Subramanian
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University of Florida
University of Florida Research Foundation Inc
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University of Florida
University of Florida Research Foundation Inc
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Application filed by University of Florida, University of Florida Research Foundation Inc filed Critical University of Florida
Priority to JP2002510412A priority Critical patent/JP2004503515A/en
Priority to CN00819645.1A priority patent/CN1250498C/en
Priority to DE60008609T priority patent/DE60008609T2/en
Priority to AT00939804T priority patent/ATE260229T1/en
Priority to EP00939804A priority patent/EP1294662B1/en
Priority to PCT/US2000/016127 priority patent/WO2001096266A1/en
Publication of WO2001096266A1 publication Critical patent/WO2001096266A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00—Preparation of halogenated hydrocarbons
    • C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
    • C07C17/12—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms in the ring of aromatic compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B39/00—Halogenation

Definitions

  • This invention relates to a process for increasing the fluorine content of a benzene or pyridine ring using copper fluoride.
  • BACKGROUND Fluorobenzene an agricultural chemicals intermediate, is typically produced by the reaction of aniline and sodium nitrite in the presence of hydrogen fluoride.
  • a diazonium salt intermediate is formed during this process which because of its instability adds to the cost of manufacture.
  • No. 4,394,527 discloses a process for monofluorinating a benzene nucleus comprising reacting a benzene compound in the liquid phase with argentic fluoride which is reduced to argentous fluoride during the reaction.
  • a process is provided for increasing the fluorine content of an aromatic ring selected from the group consisting of a benzene ring, a pyridine ring, a benzene ring substituted with from 1 to 3 inert substituents and a pyridine ring substituted with from 1 to 3 inert substituents.
  • the process comprises (a) contacting the aromatic ring with a metal fluoride composition comprising cupric fluoride (CuF 2 ) at a temperature above 250°C sufficient to transfer F from cupric fluoride to the aromatic ring, thereby chemically reducing the metal fluoride composition; (b) oxidizing the reduced metal fluoride composition from (a) in the presence of HF to regenerate a metal fluoride composition comprising cupric fluoride; and (c) employing regenerated metal fluoride composition of (b) in (a).
  • a metal fluoride composition comprising cupric fluoride (CuF 2 ) at a temperature above 250°C sufficient to transfer F from cupric fluoride to the aromatic ring, thereby chemically reducing the metal fluoride composition
  • oxidizing the reduced metal fluoride composition from (a) in the presence of HF to regenerate a metal fluoride composition comprising cupric fluoride and (c) employing regenerated metal fluoride composition of (b) in (a).
  • the regenerable reagent, cupric fluoride (C11F 2 ), is reacted with unsubstituted benzene to produce fluorobenzene.
  • Benzene may be passed over cupric fluoride at reaction conditions until an economically insufficient amount of fluorobenzene is recovered. This reaction is shown schematically in equation 1.
  • the hydrogen fluoride can be used to regenerate cupric fluoride from the copper metal as shown in equation 2.
  • the copper metal is typically reacted with HF and oxygen at a temperature of from about 250°C to about 700°C, preferably from about 375°C to about 425°C. Pure oxygen, air or oxygen diluted with inert gases such as nitrogen or argon may be used along with the HF.
  • the regeneration reaction is normally done at atmospheric pressure or slightly above atmospheric pressure for about 1 to about 24 hours.
  • the reaction variables- such as time, temperature and oxygen flow can be balanced one against the other to optimize the reaction of copper to copper fluoride. For example, as the air flow and temperature are increased, the reaction time is decreased.
  • the regenerated metal fluoride composition may then be recycled for contact with additional benzene.
  • This embodiment may be viewed as at least partially regenerating the metal fluoride composition in situ.
  • the contacting of benzene with cupric fluoride (CuF 2 ), HF and oxygen in the vapor phase is done at a temperature of at least about 250°C.
  • the reaction pressure can be subatmospheric, atmospheric or superatmospheric; generally near atmospheric pressures are preferred.
  • the contact time is typically from about 1 to about 120 seconds (e.g., from about 5 to 60 seconds).
  • the reaction can also be done in the presence of inert gases which are stable under the reaction conditions such as nitrogen and argon.
  • Unreacted benzene can be recycled to the reactor for the production of additional fluorobenzene.
  • the fluorobenzene may be recovered from the reaction product and any unreacted benzene by conventional procedures such as distillation.
  • Unsupported cupric fluoride may be used as the metal fluoride composition.
  • Supported cupric fluoride may also be used. Suitable supports include those selected from the group consisting of fluorided alumina, fluorided magnesia, fluorided calcia and oxidatively stable carbon.
  • fluorided alumina a composition comprising aluminum, oxygen and fluorine.
  • the fluoride content of the fluorided alumina can vary over a wide range, from about 0.001% to about 67.9% by weight.
  • fluorided magnesia a composition comprising magnesium, oxygen and fluorine.
  • the fluoride content of the fluorided magnesia can vary over a wide range, from about 0.001 % to about 61.0% by weight.
  • fluorided calcia is meant a composition comprising calcium, oxygenand " fluorine.
  • the fluoride content of the fluorided calcia can vary over a wide range, from about 0.001% to about 48.7% by weight.
  • Oxidatively stable carbons are described in International Publication Number WO 97/30932.
  • Particularly preferred carbons include three dimensional matrix porous carbonaceous materials. Examples are those described in U.S. Patent No. 4,978,649, which is hereby incorporated by reference herein in its entirety.
  • three dimensional matrix carbonaceous materials which are obtained by introducing gaseous or vaporous carbon-containing compounds (e.g., hydrocarbons) into a mass of granules of a carbonaceous material (e.g., carbon black); decomposing the carbon-containing compounds to deposit carbon on the surface of the granules; and treating the resulting material with an activator gas comprising steam to provide a porous carbonaceous material.
  • a carbon-carbon composite material is thus formed.
  • Example substituents include F, CF 3 , COOH, COOR, CONH 2 , CONR i R 2 , CN, CHO, NO 2 , NH 2 , OCH 3 , OCF 3 , OCCI 3 , OH and CC1 3 , where R, R and R 2 are independently selected from C j to Cg linear or branched alkyl groups.
  • substituted benzenes suitable for fluorination are fluorobenzene and trifluoromethylbenzene.
  • Examples of substituted pyridines suitable for fluorination are fluoropyridines and trifluoromethylpryidines.
  • the reaction zone and its associated feed lines, effluent lines and associated units should be constructed of materials resistant to hydrogen fluoride.
  • Typical materials of construction include stainless steels, in particular of the austenitic type, the well-known high nickel alloys, such as Monel ® nickel-copper alloys, Hastelloy ® nickel-based alloys and, Inconel ® nickel-chromium alloys, and copper-clad steel. Silicon carbide is also suitable for reactor fabrication.
  • Reaction products were analyzed using a Hewlett Packard 6890 Gas Chromatograph/5973Mass Spectrometer. All analyses are reported in area% and are shown in Table 1. The conversion decreased with time due to the formation of copper metal. Microscopic examination of the partially spent CuF showed the formation of copper metal on the surface of the particles.
  • CuF 2 was reacted with benzene under the same conditions as used in Example 1 to form fluorobenzene. At the end of the reaction all the CuF 2 was converted to copper metal. The copper metal formed was left in the reactor and treated with anhydrous HF and O 2 for 6 hours at 400°C. X-ray analysis of the product showed the formation of CuF 2 . The regenerated CuF 2 was again reacted with benzene to form fluorobenzene. For the same amount of N 2 benzene flow through the reactor, it was noted that the conversion of fluorobenzene at 550°C was about 30% for a single-pass, which is nearly twice that of the previous run.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyridine Compounds (AREA)

Abstract

A process is provided for increasing the fluorine content of benzene or pyridine rings which are optionally substituted with from 1 to 3 inert substituents. The process involves (a) contacting the ring with a metal fluoride composition comprising cupric fluoride (CuF2) at a temperature above 250 °C sufficient to transfer F from cupric fluoride to the optionally substituted ring, thereby chemically reducing the metal fluoride compositions; (b) oxidizing the reduced metal fluoride composition from (a) in the presence of HF to regenerate a metal fluoride compposition comprising cupric fluoride; and (c) employing regenerated metal fluoride composition of (b) in (a).

Description

TITLE PROCESSES FOR FLUORINATING AROMATIC RING COMPOUNDS FIELD OF THE INVENTION This invention relates to a process for increasing the fluorine content of a benzene or pyridine ring using copper fluoride.
BACKGROUND Fluorobenzene, an agricultural chemicals intermediate, is typically produced by the reaction of aniline and sodium nitrite in the presence of hydrogen fluoride. A diazonium salt intermediate is formed during this process which because of its instability adds to the cost of manufacture. U.S. Patent
No. 4,394,527 discloses a process for monofluorinating a benzene nucleus comprising reacting a benzene compound in the liquid phase with argentic fluoride which is reduced to argentous fluoride during the reaction.
There is still a need for an efficient commercial processes for preparing fluorobenzene or, more generally, fluorinating compounds having a benzene nucleus using less expensive materials.
SUMMARY OF THE INVENTION A process is provided for increasing the fluorine content of an aromatic ring selected from the group consisting of a benzene ring, a pyridine ring, a benzene ring substituted with from 1 to 3 inert substituents and a pyridine ring substituted with from 1 to 3 inert substituents. The process comprises (a) contacting the aromatic ring with a metal fluoride composition comprising cupric fluoride (CuF2) at a temperature above 250°C sufficient to transfer F from cupric fluoride to the aromatic ring, thereby chemically reducing the metal fluoride composition; (b) oxidizing the reduced metal fluoride composition from (a) in the presence of HF to regenerate a metal fluoride composition comprising cupric fluoride; and (c) employing regenerated metal fluoride composition of (b) in (a).
DETAILED DESCRIPTION In one embodiment of this invention the regenerable reagent, cupric fluoride (C11F2), is reacted with unsubstituted benzene to produce fluorobenzene. Benzene may be passed over cupric fluoride at reaction conditions until an economically insufficient amount of fluorobenzene is recovered. This reaction is shown schematically in equation 1. C6H6 + CuF2 -> C6H5F + HF + Cu° (metal) (1)
The hydrogen fluoride can be used to regenerate cupric fluoride from the copper metal as shown in equation 2.
Cu° (metal) + 2HF + l/2O2 → CuF2 + H2O (2) The copper metal is typically reacted with HF and oxygen at a temperature of from about 250°C to about 700°C, preferably from about 375°C to about 425°C. Pure oxygen, air or oxygen diluted with inert gases such as nitrogen or argon may be used along with the HF. The regeneration reaction is normally done at atmospheric pressure or slightly above atmospheric pressure for about 1 to about 24 hours. The reaction variables- such as time, temperature and oxygen flow can be balanced one against the other to optimize the reaction of copper to copper fluoride. For example, as the air flow and temperature are increased, the reaction time is decreased. The regenerated metal fluoride composition may then be recycled for contact with additional benzene.
In another embodiment of this invention a mixture of benzene, HF and oxygen are contacted with the metal fluoride composition comprising cupric fluoride at reaction conditions. The overall reaction is shown schematically in equation 3. C6H6 + HF + l/2O2 → C6H5F + H2O (3)
This embodiment may be viewed as at least partially regenerating the metal fluoride composition in situ.
The contacting of benzene with cupric fluoride (CuF2), HF and oxygen in the vapor phase is done at a temperature of at least about 250°C. The reaction pressure can be subatmospheric, atmospheric or superatmospheric; generally near atmospheric pressures are preferred.
The contact time is typically from about 1 to about 120 seconds (e.g., from about 5 to 60 seconds).
The reaction can also be done in the presence of inert gases which are stable under the reaction conditions such as nitrogen and argon.
Unreacted benzene can be recycled to the reactor for the production of additional fluorobenzene. The fluorobenzene may be recovered from the reaction product and any unreacted benzene by conventional procedures such as distillation. Unsupported cupric fluoride may be used as the metal fluoride composition. Supported cupric fluoride may also be used. Suitable supports include those selected from the group consisting of fluorided alumina, fluorided magnesia, fluorided calcia and oxidatively stable carbon.
By fluorided alumina is meant a composition comprising aluminum, oxygen and fluorine. The fluoride content of the fluorided alumina can vary over a wide range, from about 0.001% to about 67.9% by weight. By fluorided magnesia is meant a composition comprising magnesium, oxygen and fluorine. The fluoride content of the fluorided magnesia can vary over a wide range, from about 0.001 % to about 61.0% by weight. By fluorided calcia is meant a composition comprising calcium, oxygenand" fluorine. The fluoride content of the fluorided calcia can vary over a wide range, from about 0.001% to about 48.7% by weight.
Oxidatively stable carbons are described in International Publication Number WO 97/30932. Particularly preferred carbons include three dimensional matrix porous carbonaceous materials. Examples are those described in U.S. Patent No. 4,978,649, which is hereby incorporated by reference herein in its entirety. Of note are three dimensional matrix carbonaceous materials which are obtained by introducing gaseous or vaporous carbon-containing compounds (e.g., hydrocarbons) into a mass of granules of a carbonaceous material (e.g., carbon black); decomposing the carbon-containing compounds to deposit carbon on the surface of the granules; and treating the resulting material with an activator gas comprising steam to provide a porous carbonaceous material. A carbon-carbon composite material is thus formed. While the above description has been provided in the context of benzene fluorination, it will be recognized that the procedure can also be used to fluorinate pyridine or to fluorinate benzene or pyridine which is partially substituted with inert substituents (i.e., substituents which are inert under the conditions of the fluorination). Reference is made to U.S. Patent No. 5,756,834 for representative substituents (chlorine excepted) considered inert under fluorination conditions. Example substituents include F, CF3, COOH, COOR, CONH2, CONRiR2, CN, CHO, NO2, NH2, OCH3, OCF3, OCCI3, OH and CC13, where R, R and R2 are independently selected from C j to Cg linear or branched alkyl groups. Examples of substituted benzenes suitable for fluorination are fluorobenzene and trifluoromethylbenzene. Examples of substituted pyridines suitable for fluorination are fluoropyridines and trifluoromethylpryidines.
The reaction zone and its associated feed lines, effluent lines and associated units should be constructed of materials resistant to hydrogen fluoride. Typical materials of construction, well-known to the fluorination art, include stainless steels, in particular of the austenitic type, the well-known high nickel alloys, such as Monel® nickel-copper alloys, Hastelloy® nickel-based alloys and, Inconel® nickel-chromium alloys, and copper-clad steel. Silicon carbide is also suitable for reactor fabrication.
Without further elaboration, it is believed that one skilled in the art can, using the description herein, utilize the present invention to its fullest extent. The following embodiments are to be construed as illustrative, and not as consfraining the remainder of the disclosure in any way whatsoever. EXAMPLES EXAMPLE 1 Preparation of Fluorobenzene An Inconel® nickel alloy tube reactor was packed with cupric fluoride (CuF2, 5 g). The catalyst was heated to reaction temperature under a nitrogen flow. The nitrogen flow was adjusted to 20 cc/min. and benzene was then passed through a vaporizer over the catalyst at a 2 mL/hour flowrate. Reaction products were analyzed using a Hewlett Packard 6890 Gas Chromatograph/5973Mass Spectrometer. All analyses are reported in area% and are shown in Table 1. The conversion decreased with time due to the formation of copper metal. Microscopic examination of the partially spent CuF showed the formation of copper metal on the surface of the particles.
Table 1
TABLE 1 T (°C) %C6H5F
450 6.3
475 9.4
550 15
EXAMPLE 2
In this example, CuF2 was reacted with benzene under the same conditions as used in Example 1 to form fluorobenzene. At the end of the reaction all the CuF2 was converted to copper metal. The copper metal formed was left in the reactor and treated with anhydrous HF and O2 for 6 hours at 400°C. X-ray analysis of the product showed the formation of CuF2. The regenerated CuF2 was again reacted with benzene to form fluorobenzene. For the same amount of N2 benzene flow through the reactor, it was noted that the conversion of fluorobenzene at 550°C was about 30% for a single-pass, which is nearly twice that of the previous run.

Claims

1. A process for increasing the fluorine content of an aromatic ring selected from the group consisting of a benzene ring, a pyridine ring, a benzene ring substituted with from 1 to 3 inert substituents, and a pyridine ring substituted with from 1 to 3 inert substituents, comprising:
(a) contacting the aromatic ring with a metal fluoride composition comprising cupric fluoride at a temperature above 250°C sufficient to transfer F from cupric fluoride to the aromatic ring, thereby chemically reducing the metal fluoride composition; (b) oxidizing the reduced metal fluoride composition from (a) in the presence of HF to regenerate a metal fluoride composition comprising cupric fluoride; and
(c) employing regenerated metal fluoride composition of (b) in (a).
PCT/US2000/016127 2000-06-12 2000-06-12 Processes for fluorinating aromatic ring compounds Ceased WO2001096266A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2002510412A JP2004503515A (en) 2000-06-12 2000-06-12 Method for producing fluorinated aromatic ring compound
CN00819645.1A CN1250498C (en) 2000-06-12 2000-06-12 Process for fluorinating aromatic ring compounds
DE60008609T DE60008609T2 (en) 2000-06-12 2000-06-12 PROCESS FOR FLUORING AROMATIC RING COMPOUNDS
AT00939804T ATE260229T1 (en) 2000-06-12 2000-06-12 METHOD FOR FLUORINATION OF AROMATIC RING COMPOUNDS
EP00939804A EP1294662B1 (en) 2000-06-12 2000-06-12 Processes for fluorinating aromatic ring compounds
PCT/US2000/016127 WO2001096266A1 (en) 2000-06-12 2000-06-12 Processes for fluorinating aromatic ring compounds

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PCT/US2000/016127 WO2001096266A1 (en) 2000-06-12 2000-06-12 Processes for fluorinating aromatic ring compounds

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JP (1) JP2004503515A (en)
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AT (1) ATE260229T1 (en)
DE (1) DE60008609T2 (en)
WO (1) WO2001096266A1 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4394527A (en) * 1979-10-22 1983-07-19 American Cyanamid Company Method for the liquid phase oxidative fluorination of aromatic compounds

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4394527A (en) * 1979-10-22 1983-07-19 American Cyanamid Company Method for the liquid phase oxidative fluorination of aromatic compounds

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ZWEIG, ARNOLD ET AL: "New method for selective monofluorination of aromatics using silver difluoride", J. ORG. CHEM. (1980), 45(18), 3597-603, XP002160088 *

Also Published As

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CN1454195A (en) 2003-11-05
DE60008609D1 (en) 2004-04-01
JP2004503515A (en) 2004-02-05
CN1250498C (en) 2006-04-12
EP1294662B1 (en) 2004-02-25
DE60008609T2 (en) 2005-01-05
ATE260229T1 (en) 2004-03-15
EP1294662A1 (en) 2003-03-26

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