GB770640A - Manufacture of aliphatic fluorine compounds - Google Patents

Manufacture of aliphatic fluorine compounds

Info

Publication number
GB770640A
GB770640A GB825953A GB825953A GB770640A GB 770640 A GB770640 A GB 770640A GB 825953 A GB825953 A GB 825953A GB 825953 A GB825953 A GB 825953A GB 770640 A GB770640 A GB 770640A
Authority
GB
United Kingdom
Prior art keywords
aluminium
fluoride
hydrogen fluoride
copper
catalyst
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
GB825953A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst AG
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 Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB770640A publication Critical patent/GB770640A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/013Preparation of halogenated hydrocarbons by addition of halogens
    • C07C17/04Preparation of halogenated hydrocarbons by addition of halogens to unsaturated halogenated hydrocarbons
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/06Halogens; Compounds thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/20Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
    • C07C17/202Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
    • C07C17/206Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being HX
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/20Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
    • C07C17/21Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms with simultaneous increase of the number of halogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

Aliphatic fluorine compounds in which halogen (other than fluorine) has been replaced by fluorine are obtained by reacting hydrogen fluoride vapour with the vapour of a halogenated aliphatic hydrocarbon containing one or more halogen atoms other than fluorine and which may additionally contain one or more fluorine atoms in the presence of a catalyst which consists of or comprises aluminium fluoride at a temperature within the range of 300 DEG to 700 DEG C. The halogenated aliphatic hydrocarbon is preferably saturated and the process may be carried out in a continuous or discontinuous manner. In a modification of the process a halogenated ethylene containing halogen other than fluorine but which may additionally contain fluorine is reacted in the vapour phase in the presence of an aluminium fluoride catalyst with hydrogen fluoride and, if desired, chlorine, at a temperature within the range of 300 DEG to 500 DEG C. to produce a fluorinated ethane. The catalyst may comprise aluminium fluoride alone or aluminium fluoride in admixture with magnesium fluoride or with a copper halide, particularly copper fluoride. The catalyst may be obtained by passing hydrogen fluoride over small pieces of metallic aluminium or over pieces of porous alumina at raised temperature or by treating aluminium or porous aluminium oxide and copper or magnesium metal, or porous aluminium oxide impregnated with a solution of a soluble salt of copper or magnesium, e.g. a halide, sulphate, nitrate, or acetate of the metal, with hydrogen fluoride at elevated temperature (see Group III). The reaction vessel may be a tube made of nickel or of steel coated with nickel. In examples: (1) hydrogen fluoride is passed at elevated temperature through a nickel tube filled with aluminium turnings and over the aluminium fluoride formed is passed at elevated temperature a mixture of the vapours of hydrogen fluoride and carbon tetrachloride to form a product consisting of a mixture of difluorodichloromethane, trifluorochloromethane, and monofluorotrichloromethane; (2) as in (1) except that the catalyst is formed by passing hydrogen fluoride over porous alumina at elevated temperature; (3) as in (2) except that the alumina is impregnated with magnesium chloride solution, a smaller amount of trifluoromonochloro methane being obtained in this case; (4) as in (1) except that the catalyst is made by treating a mixture of porous alumina and copper turnings with hydrogen fluoride at elevated temperature, an increased amount of trifluorochloromethane being obtained in this case; it is stated that when no copper turnings are added some tetrafluoromethane is formed; (5) as in (3) except that the alumina is impregnated with a cuprous chloride solution, a considerably increased yield of trifluoro chloromethane being obtained in this case and no tetrafluoromethane being formed; (6) as in (5) except that difluorodichloromethane is used instead of carbon tetrachloride, the product in this case being trifluoromethane; (7) a mixture of tetrachlorethylene, chlorine and hydrogen fluoride is passed at 400-450 DEG C. over the catalyst obtained as in (2) to form 1 : 1 : 2-trifluoro-1 : 2 : 2-trichloroethane and a small amount of 1,2-difluoro-tetrachlorethane. Reference is also made to the reaction of trichlorethylene with hydrogen fluoride in the presence of aluminium fluoride catalyst to form 1 : 1 : 1-trifluoro 2-chlorethane.ALSO:An aluminium fluoride catalyst used in the production of aliphatic fluorine compounds by reacting a halogenated aliphatic hydrocarbon containing one or more halogen atoms other than fluorine with hydrogen fluoride (see Group IV(b)) may comprise aluminium fluoride obtained by passing hydrogen fluoride over small pieces of metallic aluminium or porous alumina at elevated temperature or may comprise a mixture of aluminium fluoride with magnesium fluoride or with a copper halide, particularly copper fluoride. Suitable mixed catalysts may be obtained by treating aluminium or porous aluminium oxide and copper or magnesium metal, or porous aluminium oxide impregnated with a solution of a soluble salt of copper or magnesium, e.g. a halide, sulphate, nitrate, or acetate, with hydrogen fluoride at elevated temperature. An alloy of aluminium with magnesium or copper may be used for the treatment with hydrogen fluoride. In the examples the catalysts used are prepared by (1) passing hydrogen fluoride vapour at elevated temperature through a nickel tube filled with aluminium turnings; (2) passing hydrogen fluoride over porous alumina at 360-400 DEG C.; (3) impregnating alumina with magnesium chloride and treating with hydrogen fluoride as in (2); (4) treating a mixture of porous alumina and copper turnings with hydrogen fluoride at a temperature rising from 80 DEG to 500 DEG C; and (5) treating alumina impregnated with a solution of cuprous chloride with hydrogen fluoride at elevated temperature.
GB825953A 1952-04-04 1953-03-25 Manufacture of aliphatic fluorine compounds Expired GB770640A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF8750A DE1000798B (en) 1952-04-04 1952-04-04 Process for the preparation of aliphatic fluorine compounds

Publications (1)

Publication Number Publication Date
GB770640A true GB770640A (en) 1957-03-20

Family

ID=7085925

Family Applications (1)

Application Number Title Priority Date Filing Date
GB825953A Expired GB770640A (en) 1952-04-04 1953-03-25 Manufacture of aliphatic fluorine compounds

Country Status (2)

Country Link
DE (1) DE1000798B (en)
GB (1) GB770640A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2946828A (en) * 1957-12-02 1960-07-26 Hoechst Ag Process for preparing aliphatic fluorine compounds
EP0439338A1 (en) * 1990-01-25 1991-07-31 Imperial Chemical Industries Plc A catalyst for halogen exchange in halohydrocarbons and for acid/base reactions
US5051538A (en) * 1988-07-29 1991-09-24 E. I. Dupont De Nemours And Company Process for 1,1-dichloro-1-fluoroethane

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2005706A (en) * 1932-08-10 1935-06-18 Kinetic Chemicals Inc Organic fluorine compound
US2456027A (en) * 1944-04-01 1948-12-14 Minnesota Mining & Mfg Method of making fluorocarbons
US2478201A (en) * 1947-04-02 1949-08-09 Allied Chem & Dye Corp Disproportionation of fluoro-halogeno derivatives of methane in presence of aluminumfluoride
US2576823A (en) * 1947-11-13 1951-11-27 Du Pont Fluorination with granular crf3 catalyst
US2471525A (en) * 1947-12-19 1949-05-31 Phillips Petroleum Co Reaction of an acetylene with hf to produce vinyl fluoride and/or difluoroethane andhomologues thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2946828A (en) * 1957-12-02 1960-07-26 Hoechst Ag Process for preparing aliphatic fluorine compounds
US5051538A (en) * 1988-07-29 1991-09-24 E. I. Dupont De Nemours And Company Process for 1,1-dichloro-1-fluoroethane
EP0439338A1 (en) * 1990-01-25 1991-07-31 Imperial Chemical Industries Plc A catalyst for halogen exchange in halohydrocarbons and for acid/base reactions
AU639744B2 (en) * 1990-01-25 1993-08-05 Imperial Chemical Industries Plc A catalyst for halogen exchange in halohydrocarbons and for acid/base reactions

Also Published As

Publication number Publication date
DE1000798B (en) 1957-01-17

Similar Documents

Publication Publication Date Title
JP5143011B2 (en) Method for producing fluorinated organic compound
US3258500A (en) Process for fluorinating halohydro-carbons
JP2024105492A (en) Method for producing fluorinated organic compounds
CA2608327C (en) Processes for selective dehydrohalogenation of halogenated alkanes
JP5926488B2 (en) Process for producing fluorinated olefins
US2744148A (en) Process for fluorination of haloalkanes using a hydrogen fluoride activated catalyst containing alumina, a metal fluoride and basic aluminum fluoride
JPH01221338A (en) Gaseous phase fluorination
JP6827246B2 (en) Method for producing halogenated butene compound
WO2016078225A1 (en) Trans-1,1,1,4,4,4-hexafluoro-2-butene synthesis method
DE68904482T2 (en) METHOD FOR HYDROFLUORING IN THE GAS PHASE.
US2744147A (en) Fluorination of haloalkanes with a catalyst containing gamma alumina
US5177273A (en) Process for the manufacture of halogen-substituted propanes containing hydrogen and at least five fluorine substituents
US5545774A (en) Process for the manufacture of 1,1,1,3,3,3-hexafluoropropane
US3651156A (en) Process for the manufacture of fluorinated aliphatic hydrocarbon compounds
US2478932A (en) Manufacture of 1, 1, 1-trifluoroethane
GB770640A (en) Manufacture of aliphatic fluorine compounds
WO2007056149A1 (en) Method for producing fluorinated organic compounds
US2379414A (en) Manufacture of unsaturated halogen-containing compounds
US2327174A (en) Preparation of halogenated olefins
TW202035349A (en) Method for producing cyclobutene
US2377669A (en) Perchlorination process
US2946828A (en) Process for preparing aliphatic fluorine compounds
US3456025A (en) Preparation of difluoroalkenes
GB745818A (en) Improvements in or relating to a process for producing fluorohalo-derivatives of saturated aliphatic hydrocarbons
JP7208976B2 (en) Method for producing fluorine-containing sulfide compound