Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C17/00—Preparation of halogenated hydrocarbons
  • C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
  • C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
  • C07C17/278—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of only halogenated hydrocarbons

Definitions

• the present invention relates to a process for the preparation of halogenated hydrocarbons comprising at least 3 carbon atoms by catalytic reaction between a haloalkane and an olefin.
• the addition of a haloalkane to an olefin is a well known reaction.
• Patent application WO 97/07083 describes a process for the preparation of halogenated hydrocarbons under the catalytic action of cuprous chloride in the presence of t.butylamine as cocatalyst. In such a process, the yield of telomerization product is however quite low.
• Patent application EP-A-787 707 describes a process for the preparation of 1,1,1,3,3-pentachlorobutane under the catalytic action of cuprous chloride in the presence of cocatalysts of the amino type.
• the yield and selectivity of the telomerization product are not, however, excellent.
• the present invention aims to provide a telomerization process for preparing halogenated hydrocarbons comprising at least 3 carbon atoms by catalytic reaction between a haloalkane and an olefin with improved yields and selectivities.
• the invention relates to a process for the preparation of halogenated hydrocarbons comprising at least 3 carbon atoms in which a haloalkane and an olefin are reacted in the presence of a catalyst in a reaction medium, a process in which the reaction medium is essentially free of water.
• the reaction medium comprises at least the catalyst, the haloalkane and the olefin.
• the reaction medium can further comprise, for example, a cocatalyst and / or a solvent, preferably a cocatalyst.
• the reaction medium generally contains at most 1300 mg / kg of water. Often, the reaction medium contains at most 1000 mg / kg of water. A reaction medium containing at most 700 mg / kg of water is very suitable. Preferably the reaction medium contains at most 400 mg / kg of water. A reaction medium containing at most 300 mg / kg of water is very particularly preferred.
• the process can of course be carried out in a completely anhydrous reaction medium. However, it has been found that the presence of traces of water in small quantities is not a problem. Typically, the process according to the invention is carried out with a reaction medium containing more than 20 mg / kg of water, or even more than 50 mg / kg of water.
• the water content of the reaction medium can be controlled, for example, by removing traces of water from the reactor used.
• One can, for example, prior to the introduction of the reaction medium, heat the reactor and / or perform purges of the reactor with a dry gas.
• Operations which can be used to reduce the water content in the constituents of the reaction medium are, for example, a drying operation, such as for example adsorption on a solid adsorbent or a distillation operation.
• a variant of the process according to the invention therefore relates to a process in which
• This variant is particularly useful when at least one fraction of a reaction mixture resulting from the step in which the olefin and the haloalkane are reacted in the presence of a catalyst containing reagents not consumed is subjected to at least one treatment with an aqueous medium. If applicable treatment with the aqueous medium aims in particular to stop the reaction between the olefin and the haloalkane and to separate the catalyst and optionally the cocatalyst from the other constituents of the reaction medium.
• the cocatalyst is isolated from the aqueous medium by a separation operation such as, for example, stripping or distillation and, if necessary, the separated cocatalyst is subjected to an additional treatment for reducing the water content before recycling. towards the reaction between olefin and haloalkane.
• the fraction subjected to the reduction treatment of the water content may contain unconsumed reagents (olefin and / or haloalkane), catalyst, cocatalyst, solvent or mixtures of these compounds. In a preferred variant, it contains olefin. In another preferred variant, it contains cocatalyst. In yet another variant, it contains haloalkane.
• the process according to the invention can be a continuous or discontinuous process. In a batch process, it is preferable to carry out a gradual addition to the reaction medium during the reaction of at least part of at least one reagent selected from olefin, and haloalkane and optionally the cocatalyst and / or the solvent.
• the catalyst can be chosen from the metal derivatives known to catalyze the reaction of a haloalkane with an olefin.
• metal derivatives known to catalyze the reaction of a haloalkane with an olefin.
• examples include the salts and organic compounds of the metals in groups VIA, NIIA, VIII and IB of the periodic system of the elements. Among these metals, nickel, iron and copper give good results. Copper compounds are well suited as a catalyst. Copper salts and organic copper compounds are particularly preferred as the catalyst.
• Such catalysts are described, for example, in patent applications WO-A-98/50329 and WO-A-98/50330, the content of which is incorporated by reference. Copper (I) chloride, copper (II) chloride or copper (II) acetylacetonate give good results. Hydrated copper salts can be used provided that they do not introduce into the reaction medium a water content greater than the content specified above.
• anhydrous copper salts it is preferred to use anhydrous copper salts.
• an anhydrous copper (II) salt is used.
• an anhydrous copper (II) salt chosen from halides or copper (II) acetate, in particular anhydrous copper (II) chloride.
• the reaction is preferably carried out in the presence of a cocatalyst selected, for example, from the group consisting of amines and trialkylphosphine oxides.
• an amine as a cocatalyst, in particular a primary amine.
• Amines which can be used are in particular t.butylamine and the tert-alkyl amines PRIMENE® 81-R and JM-T sold by Rohm and Haas Company. T.butylamine, the amines PRIMENE® 81 -R and PRIMENE® JM-T are very particularly preferred.
• the PRIMENE® 81-R amine is a mixture of tert.-alkyl primary amines with a number of carbon atoms from 12 to 14.
• the PRIMENE® JM-T amine is a mixture of tert primary amines. -alkyl whose number of carbon atoms is from 18 to 22.
• trialkylphosphine oxides which can be used as cocatalyst, there may be mentioned in particular the compounds of formula (RlR2R3) PO, in which RI, R2 and R3 represent identical or different, preferably linear, C3-C10 alkyl groups.
• RI, R2 and R3 represent identical or different, preferably linear, C3-C10 alkyl groups.
• the catalyst-cocatalyst system preferred in the process according to the invention is the system consisting of a copper compound and a primary amine in which the carbon atom neighboring the group NH2 is a quaternary carbon atom, that is to say that is, without a hydrogen atom.
• Particularly preferred are the catalyst-cocatalyst systems formed by copper (II) acetylacetonate and t.butylamine or by copper (II) chloride and t.butylamine.
• a particularly preferred catalyst-cocatalyst system is the system formed by copper (II) acetylacetonate and PRIMENE®JM-T.
• the reaction is preferably carried out in the absence of solvent. However, the reaction can also be carried out in the presence of a solvent. Any solvent in which the reactants form the desired product with a satisfactory yield can be used.
• the haloalkanes used in the process according to the present invention are generally saturated organic compounds. They preferably have from one to three carbon atoms. Often they contain at least 2 chlorine atoms. Haloalkanes in which at least 2 chlorine atoms are linked to the same carbon atom give good results. Haloalkanes comprising a dichloromethyl or trichloromethyl group are preferred. As examples of haloalkanes according to the present invention include dichl oromethane, chloroform, carbon tetrachloride, 1,1,1-trichloroethane. Carbon tetrachloride is very particularly preferred.
• the haloalkanes may also include other substituents such as other halogen atoms, alkyl or haloalkyl groups. However, haloalkanes containing only chlorine as the halogen are preferred.
• the olefin used in the process according to the present invention is generally an ethylene, a propylene or a butene, optionally substituted with a substituent.
• the substituents are chosen, for example, from halogen atoms, alkyl or haloalkyl groups, nitrile (CN) or carboxylic acid (COOH) groups.
• Halogenated olefins are particularly suitable. Among the halogenated olefins, chlorinated olefins give good results. Chlorinated olefins which can be used in the process according to the invention generally correspond to the general formula
• R1C1C CR2R3
• R1, R2 and R3 independently represent an H or Cl atom, an alkyl or alkenyl group, linear, cyclic or branched, optionally substituted, or an aryl or heteroaryl group, optionally substituted.
• chlorinated olefins mention may be made of vinyl chloride, vinylidene chloride, trichlorethylene, the various isomers of chloropropenes such as 1-chloroprop-1-ene, 2-chloroprop-1-ene and 3-chloroprop-1-ene. Excellent results can be obtained with vinyl chloride and 2-chloroprop-1-ene.
• the halogenated hydrocarbons obtained according to the process of the present invention generally belong to the family of chlorinated alkanes comprising at least three carbon atoms. These are often chloropropanes, chlorobutanes or chloropentanes.
• the carbon atoms of said chloropropanes, chlorobutanes and chloropentanes can also be substituted by other functional groups, such as, for example, alkyl or aryl groups, nitrile (CN) or carboxylic acid (COOH) groups.
• halogenated hydrocarbons contain only chlorine as the halogen. Chloropropanes and chlorobutanes unsubstituted by other functional groups are preferred.
• the halogenated hydrocarbons obtained according to the process of the present invention correspond to the general formula CnH (2n + 2) -pClp in which n is an integer and has the values 3 or 4, p is an integer which has the values 3 to 7.
• Examples of compounds obtained according to the process of the present invention are 1,1,1,3,3 -pentachloropropane, 1,1,2,3,3-pentachloropropane, 1,1,1,3,3-pentachl orobutane, 1,1,1,3- tetrachloropropane, 1,1,3,3- tetrachlorobutane, 1,1,1,3,3,3-hexachlororopropane and 1,1-dichloro-2-trichloromethylpropane.
• 1,1,1,3,3-pentachloropropane, 1,1,1,3,3-pentachlorobutane and 1,1,1,3,3,3-hexachlororopropane are preferred.
• 1,1,1,3,3-pentachlorobutane and 1,1,1,3,3-pentachloropropane are very particularly preferred.
• the reaction medium is maintained at a temperature and a pressure sufficient to allow the catalytic reaction of the haloalkane with the olefin.
• the preferred reaction conditions in the process according to the invention with regard to temperature, pressure, duration and the ratio between the constituents of the reaction medium, etc. are described in patent application WO-A-98/50330, the content of which is incorporated by reference.
• halogenated hydrocarbons obtained according to the process of the invention are precursors of the corresponding fluorinated analogs, which can be easily obtained by treatment with hydrogen fluoride, preferably anhydrous, optionally in the presence of a fluorination catalyst such as for example an antimony salt, a titanium salt, a tantalum salt or a tin salt. Halides are preferred as the salt of said metals.
• fluorination catalysts which can be used are chosen from compounds, preferably oxides, of chromium, of alumina and of zirconium.
• fluorinated hydrocarbons correspond to the formula C n H (2n + 2) -pFp in which n is an integer and has the values 3 or 4 and p is an integer which has the values 3 to 7.
• Des preferred fluorinated hydrocarbons are chosen from 1,1,1,3,3-pentafluorpropane, 1,1,1,3,3,3-hexafluorpropane and 1,1,1,3,3, - pentafluorbutane.
• the invention therefore also relates to a method for obtaining a fluorinated hydrocarbon comprising (a) the synthesis of a halogenated hydrocarbon according to the process according to the invention and (b) a treatment of the halogenated hydrocarbon derived from (a ) with hydrogen fluoride as described above.
• Examples 1-4 1,1,1,3,3-Pentachlorobutane was prepared by reaction between 2-chloroprop-1-ene (2-CPe) and carbon tetrachloride in the presence of cupric chloride and t-butylamine (tBu) in the presence of varying amounts of water.
• the reagents (2-CPe, CC1 4 ), the catalyst (CuCl 2 ) and the amine (tBu) were introduced into a penicillin-type glass flask in molar ratios 2- CPe / CC / CuCVtBu 1/2 / 0.002 / 0.1 and a certain amount of water was added.
• 1,1,1,3,3-Pentachlorobutane was prepared by reaction, in a substantially anhydrous medium, between 2-chloroprop-1-ene (2-CPe) and carbon tetrachloride in the presence of copper acetylacetonate, and amine Primene JM-T ® (Rohm & Haas).
• the reactants (2- CPe, CC1), the catalyst (Cu (acac) 2 ) and Famine (JM-T) were introduced into a reactor in molar ratios 2-CPe / CCl 4 / Cu (acac ) 2 / JM-T of 1/2 / 0.001 / 0.22.
• the reactor was then heated to 90 ° C.

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• 2000
  • 2000-09-26 WO PCT/EP2000/009490 patent/WO2001025176A1/fr not_active Ceased
  • 2000-09-26 AT AT00967818T patent/ATE267790T1/de not_active IP Right Cessation
  • 2000-09-26 ES ES00967818T patent/ES2220547T3/es not_active Expired - Lifetime
  • 2000-09-26 AU AU77845/00A patent/AU7784500A/en not_active Abandoned
  • 2000-09-26 DE DE60011118T patent/DE60011118T2/de not_active Expired - Lifetime
  • 2000-09-26 EP EP00967818A patent/EP1222154B1/fr not_active Expired - Lifetime
  • 2000-09-26 JP JP2001528127A patent/JP2004500339A/ja active Pending
  • 2000-09-29 US US09/677,127 patent/US6369285B1/en not_active Expired - Lifetime

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