GB581254A - Improvements in or relating to the production of organic fluorine compounds - Google Patents

Improvements in or relating to the production of organic fluorine compounds

Info

Publication number
GB581254A
GB581254A GB15325/44A GB1532544A GB581254A GB 581254 A GB581254 A GB 581254A GB 15325/44 A GB15325/44 A GB 15325/44A GB 1532544 A GB1532544 A GB 1532544A GB 581254 A GB581254 A GB 581254A
Authority
GB
United Kingdom
Prior art keywords
fluorine
halogenated
halogen
propene
atom
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB15325/44A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Publication of GB581254A publication Critical patent/GB581254A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/26Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
    • C07C17/272Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
    • C07C17/278Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of only halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/08Materials not undergoing a change of physical state when used
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Combustion & Propulsion (AREA)
  • Thermal Sciences (AREA)
  • Materials Engineering (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Halofluoroalkanes are prepared by reacting in the presence of a Friedel-Crafts catalyst, a halogenated methane containing at least three halogen atoms but no fluorine, with a halogenated ethylenic compound having at least one atom of chlorine attached to one of the doubly-bonded carbon atoms, said ethylenic compound also containing at least one fluorine atom. Thus, ethylenic compounds having the general formula RR1C=CR2X, where R, R1 and R2 are hydrogen, fluorine, chlorine, alkyl or chlorinated or fluorinated alkyl, at least one of these substituents being fluorine or fluorinated alkyl and X is chlorine are operable in this process. Reaction temperatures up to 150 DEG C. may be used though preferably normal or slightly elevated temperatures are used, in general from 15 DEG to 100 DEG C. The preferred catalyst is aluminium chloride though other Friedel Crafts catalysts such as boron trifluoride, zinc chloride or ferric chloride may be used. The products may be isolated by destroying the catalyst, as by decomposition with ice or cold water, followed by distillation. Specified ethylenic compounds employable in the process are 1,2 - dichloro - 3 - trifluoro - 1 - propene, 1,1,2 - trichloro - 3 - trifluoro - 1 - propene, 1 - dichloro - 3 - trifluoro - 1 - propene, 1,1,3,3,3 - pentafluoro - 2 - chloro - 1 - propene, asym.-difluorodichloroethylene, sym.-dichlorodifluoroethylene, and trifluorochloroethylene. In examples: (1) chloroform and trifluorochloroethylene were reacted in the presence of aluminium chloride in a silver-lined high-pressure tube at 50 DEG C. and from the reaction products, tetrachlorotrifluoropropane and pentachlorodifluoro propane were recovered; (2) trifluorochloroethylene and carbon tetrachloride were reacted in the presence of aluminium chloride yielding pentachlorotrifluoropropane and hexachlorodifluoropropane. The products may be used as petroleum chemicals, dialectric fluids and cooling liquids. Specification 570,470 is referred to. The Specification as open to inspection under Sect. 91 comprises also the reaction of a halogenated methane containing at least three halogen atoms with a halogenated ethylenic compound having at least one atom of halogen other than fluorine attached to one of the doubly bonded carbon atoms and containing at least one fluorine atom, while in the formula given above, R, R1 and R2 may be any halogen or halogenated alkyl and X may be halogen. This subject-matter does not appear in the Specification as accepted.
GB15325/44A 1943-08-11 1944-08-11 Improvements in or relating to the production of organic fluorine compounds Expired GB581254A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US581254XA 1943-08-11 1943-08-11

Publications (1)

Publication Number Publication Date
GB581254A true GB581254A (en) 1946-10-07

Family

ID=22014853

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15325/44A Expired GB581254A (en) 1943-08-11 1944-08-11 Improvements in or relating to the production of organic fluorine compounds

Country Status (1)

Country Link
GB (1) GB581254A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991008183A1 (en) * 1989-12-05 1991-06-13 Asahi Glass Company Ltd. Method for producing dichloropentafluoropropanes
US5220084A (en) * 1989-12-05 1993-06-15 Asahi Glass Company Ltd. Method for producing dichloropentafluoropropanes
US5227547A (en) * 1989-12-05 1993-07-13 Asahi Glass Company Ltd. Method for producing dichloropentafluoropropanes

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991008183A1 (en) * 1989-12-05 1991-06-13 Asahi Glass Company Ltd. Method for producing dichloropentafluoropropanes
US5220084A (en) * 1989-12-05 1993-06-15 Asahi Glass Company Ltd. Method for producing dichloropentafluoropropanes
US5227547A (en) * 1989-12-05 1993-07-13 Asahi Glass Company Ltd. Method for producing dichloropentafluoropropanes
US5434321A (en) * 1989-12-05 1995-07-18 Asahi Glass Company Ltd. Method for producing dichloropentafluoropropanes

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