Classifications

• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
  • C01B7/00—Halogens; Halogen acids
  • C01B7/24—Inter-halogen compounds
• • 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
  • C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
  • C07C17/202—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
  • C07C17/204—Preparation 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 a halogen

Definitions

• C 3 F 7 I is used as a raw material and a force-pulling reaction is performed using a metal such as zinc.
• This method has problems that it is difficult to obtain C 3 F 7 I to be used as a raw material and that metal iodide is by-produced.
• Method d has the advantage that it is difficult to generate partially fluorinated compounds.However, fluorine gas is rich in reactivity, and it is not easy to control the reaction temperature due to severe heat generated by the reaction, and the C-C bond is broken. As a result, the yield of the target product decreases. In addition, this method is not industrially useful because of the danger of explosion and equipment corrosion.
• an object of the present invention is to provide a new industrial production method of perfluoroalkane which can replace the conventional method in order to solve the various problems described above.
• the present inventors have conducted intensive studies on industrial production methods for monofluoroalkanes, for example, perfluorobenzene (hexafluoroethane) and perfluorohexane (tetradecafluorohexane). Using perfluoroalkyl iodides and fluorine to form perfluoroalkanes and
• the reaction to produce the IF 5 is inert to par full O b alkyl Ai Oda I de and fluorine gas, lower compared boiling with IF 5, therefore, at least partly under reaction conditions
• the reaction can be carried out in the presence of at least one liquid selected from the group consisting of a perfluoro compound, a hydrogen fluoride compound, and hydrogen fluoride, which can exist as a liquid and can be easily evaporated by the heat generated by the reaction, resulting in a huge reaction
• the calorific value can be absorbed / removed as the latent heat required to evaporate at least one liquid selected from the perfluoro compound, the chlorofluoro compound and hydrogen fluoride, thereby making the reaction temperature easy and efficient. I found that I could control it.
• the reaction temperature can be prevented from becoming excessively high. Since the degree can be controlled as predetermined, side reactions can be suppressed. In addition, since an indirect cooling device for cooling the reaction solution, which has been generally used for removing the reaction heat, may be omitted, the reaction device becomes a simple reaction device as a whole, and economically. It is advantageous.
• IF 5 simultaneously produced from the reaction, for example Ru mower advantage that it can be used as starting material for the production of par full O b alkyl Aiodi de.
• a perfluoroalkyl iodide is reacted by bringing it into contact with fluorine gas, and the general formula: R f — F (where R f — is represented by F (CF 2 ) n —) And n is an integer of from 2 to 10.
• the perfluoroalkyl iodide is used under the conditions of this method. And performing the contacting in the presence of at least one liquid selected from a perfluoro compound, a fluorinated fluorine compound, and hydrogen fluoride, which is substantially inert to fluorine gas.
• substantially inert means that when the method of the present invention is carried out, it is inert to such an extent that it does not adversely affect the advantages obtained by the method. It means there is. That is substantially inert to the reaction for producing Pafuruoro alkanes and IF 5, which means that no such adverse effect to the extent beyond the advantages obtained by the present invention to its reaction.
• FIG. 1 is a schematic flow sheet of an apparatus for performing the method of the present invention.
• reference number 1 refers to the reactor
• reference number 2 refers to the tower
• the number 3 indicates a condenser
• the reference number 4 indicates a receiver
• the reference numbers 12 and 15 indicate valves.
• the contact between the perfluoroalkyl iodide and the fluorine gas may be carried out by any method that allows both components to coexist and react.
• at the time of the reaction at least one liquid selected from a perfluoro compound, a fluorinated fluoro compound and hydrogen fluoride exists. .
• to promote the contact between the two reaction components and such liquids eg by stirring, etc.
• perfluoroalkyl iodide and fluorine gas are supplied as a liquid to at least one liquid selected from a perfluoro compound, a fluorinated fluoro compound and hydrogen fluoride (either mechanically mixed or Need not be mixed);
• Perfluoro compound as a liquid adjacent to at least one liquid phase selected from a perfluoro compound, a fluorinated compound and hydrogen fluoride
• the mode of supplying the liquid adjacently means, for example, adjacent to the falling phase of at least one liquid selected from a perfluoro compound, a halogenated fluorine compound and hydrogen fluoride (for example, without mechanically mixing positively).
• these reactants are supplied (simply supplied in the falling phase) can be used.
• the reactants are supplied in countercurrent or cocurrent with each other to the liquid falling phase. Both are possible.
• a gaseous or liquid reactant is supplied into the column with respect to at least one liquid selected from a perfluoro compound, a fluorinated fluorine compound and hydrogen fluoride flowing down in the packed column. Is equivalent to Even without active mechanical mixing, the presence of the packing causes gas-liquid and Z or liquid-liquid contact, whereby the reactants and such liquids spontaneously mix with each other. Needless to say.
• the reaction caused by the contact mainly comprises the formula:
• R f has the same meaning as described above.
• the present invention provides a method for producing a perfluoroalkane represented by the general formula: R f —F, wherein the reaction:
• R f has the same meaning as described above.
• Fluoro compounds and hydrogen fluoride A method characterized in that the method is carried out in the presence of at least one liquid selected from the group consisting of:
• the heat of reaction generated by the reaction is at least one liquid selected from the group consisting of a perfluoro compound, a fluorinated compound and hydrogen fluoride present as a liquid in the reaction system.
• reaction system refers to a state in which a reaction can occur in the presence of a reactant, a force in which a reaction is actually occurring, or a part in a state in which both are present.
• the evaporated compound may be removed from the reaction system and condensed, or may be condensed in the reaction system.
• Such a method of removing heat of reaction using latent heat of vaporization can directly remove heat from the reaction system as compared with indirect heat exchange generally used for heat removal from the reaction system.
• it since it can be removed as latent heat instead of sensible heat, it is advantageous in that a larger amount of heat can be removed using at least one liquid selected from a smaller amount of a perfluoro compound, a fluorine compound, and hydrogen fluoride.
• At least one liquid selected from the condensed perfluorinated compound, macrofluorinated compound and hydrogen fluoride may be returned to the reaction system and used again for heat removal.
• At least one liquid selected from the group consisting of a perfluoro compound, a fluorinated compound, and hydrogen fluoride that is usable is substantially inert to fluorine gas under the reaction conditions,
• a perfluoro compound, a fluorinated compound, and hydrogen fluoride that is usable is substantially inert to fluorine gas under the reaction conditions.
• At least one liquid compound selected from the perfluoro compound, the fluorinated compound and hydrogen fluoride is selected from the perfluoro compound, the fluorinated compound and hydrogen fluoride
• perfluoro or chloro-fluoroalkanes eg, perfluoro-rotan, no, .one-fluoroprono, .n, no, "one-fluorobutane, no, 'one-fluoro-hexane, dichlorodifluoromethane, triclo. , Fluorotrichloromethane, dichlorotetrafluoroethane, etc.
• perfluorocycloalkanes eg perfluorocyclobutane, no, "one fluorocyclopentane, no. one fluorocyclohexane, no. one fluorodecalin, etc.
• perfluorinated compounds and fluorine-containing perfluoro compounds particularly preferred are those having a relatively low boiling point (at atmospheric pressure), for example, those having a boiling point of 100 ° C or less, particularly, 140 to 80 ° C. C range, including those with 1 to 7 carbon atoms. Since these compounds evaporate easily, they are advantageous for removing the heat of reaction.
• the difference in boiling point between perfluoroalkane, which is the target product, and at least one liquid selected from perfluorinated compounds, fluorine-containing fluoro compounds and hydrogen fluoride is not so important.
• Whichever boiling point is high.
• the boiling point of a perfluoroalkane is high, the desired product is retained in the reaction system, and the perfluoro compound, the fluorinated compound and At least one liquid selected from hydrogen fluoride can be evaporated from the reaction system, condensed and recycled, which may be convenient in some cases.
• the perfluoroalkane may be removed from the reaction system. Evaporates at least one liquid selected from the group consisting of a fluorinated compound, a perfluoro compound, a fluorinated fluorinated compound and hydrogen fluoride, takes it out of the reaction system, and condenses them, for example, rectification, liquid separation, etc.
• the desired product, perfluoroalkyl is used as the perfluoro compound which evaporates due to the heat of reaction.
• the perfluoroalkane only evaporates and comes out of the reaction system.Therefore, the perfluoroalkane only needs to be cooled and condensed and then returned to the reaction system in the required amount.
• the separation after condensation as described above is not required.
• the third component is not mixed into the system. For example, when C 6 F 14 is produced, heat of reaction can be removed by using C 6 F 14 as a perfluoro compound.
• C 4 F 10 can be used to produce C 4 F 10 .
• the reaction conditions can be appropriately selected depending on the desired perfluoroalkane and at least one liquid selected from a perfluoro compound, a cyclofluoride compound and a hydrogen fluoride used.
• a reaction temperature of 150 to 100 ° C., an atmospheric pressure (in some cases, reduced pressure) to a reaction condition of 5 Kg / cm 2 —G can be exemplified.
• the reaction temperature is determined by using at least one liquid selected from a perfluorinated compound, a fluorinated compound and hydrogen fluoride in an amount sufficient to absorb the reaction heat and evaporate. It is preferred that the boiling point under the reaction conditions of at least one liquid selected from the group consisting of a compound of the formula (1), a compound of the formula (3), and hydrogen fluoride is substantially equal. The advantage is that it can be kept constant.
• the amount of par full O b alkyl ⁇ Iodai de with fluorine gas to react in contact is not particularly limited power?, Effectively stoichiometric to obtain par full O b alkane It is preferable to use the fluorine gas in an amount of at least the amount (ie, at least 3 moles of the fluorine gas per mole of the perfluoroalkyl iodide).
• the optimum amount of fluorine gas is generally about 3 to 5 mole times the amount of perfluoroalkyl iodide.
• the excess unreacted fluorine gas exits the reaction system as a gas, together with at least one liquid selected from evaporating perfluoro compounds, chlorofluoro compounds and hydrogen fluoride, and optionally the desired product. Go. Therefore, if a large excess of fluorine gas is used, a large-scale apparatus is required for recovery and recycling of unreacted fluorine gas, which is not economically preferable.
• At least one liquid selected from a perfluoro compound, a fluorinated fluoro compound and hydrogen fluoride, and a perfluoroalkane, which is a desired reaction product, which may be present, are usually evaporated. do it
• the reaction heat is taken out of the system by taking it out of the system, cooling it and condensing it.
• any kind of general condenser may be used.
• the desired product evaporates at the same time, and the boiling point difference between the desired product and at least one liquid selected from the group consisting of a perfluoro compound, a fluorinated fluoro compound and hydrogen fluoride.
• it is convenient to separate by condensing it because it can be separated at the same time as condensation.
• a predetermined amount of perfluoroiodide and at least one liquid selected from a perfluoro compound, a cyclofluoride compound and hydrogen fluoride is added to the reactor, and then a predetermined amount of fluorine gas is added to the reaction system, and at least one liquid selected from the group consisting of a perfluoro compound, a fluorinated fluorine compound, and hydrogen fluoride that evaporates as the reaction proceeds.
• the perfluoroalkane is removed from the reaction system and condensed, and the whole amount is returned to the reaction system and used for removing the heat of reaction in the subsequent reaction.
• At least one liquid selected from a perfluoro compound, a fluorinated fluorine compound and hydrogen fluoride is previously charged into a reactor, and Then, after heating to the predetermined reaction temperature, the reactants perfluoroalkyl iodide and fluorine gas are continuously supplied. At least one liquid selected from a perfluoro compound, a fluoro compound and hydrogen fluoride and the target product are evaporated from the reaction system by heat generated by the reaction, and are taken out of the reaction system. At least one liquid selected from perfluorinated compounds, fluorinated compounds and hydrogen fluoride is returned to the reaction system, and perfluoroalkane is continuously recovered as a product. Also, by extracting the reaction system (liquid) continuously, after then separated recovered IF 5, it is possible to return the remainder to the reaction system.
• At least one liquid selected from a perfluoro compound, a cyclofluoride compound and hydrogen fluoride is first charged into a reactor.
• the perfluoroalkyl iodide and the fluorine gas may be continuously supplied in the presence of the compound flowing down, for example, they may be supplied in the compound flowing down.
• a perfluoroalkyl iodide is added to the flowing compound, or the compound is allowed to flow down in parallel with the compound without being added to the compound, while fluorine gas is supplied in a countercurrent flow. Good.
• the reaction proceeds in the compound while at least one liquid selected from a perfluoro compound, a fluorinated fluorine compound and hydrogen fluoride flows down, and some of the compound evaporates due to heat of reaction.
• the desired product may also evaporate.
• the reactor Pas - Furuoro compound, at least selected from black port Furuoro compound and hydrogen fluoride one liquid and IF 5 is also possible to make substantially present.
• the reactor for carrying out the method of the present invention comprises a reactor accommodating the reaction system and at least one liquid selected from a perfluoro compound, a fluorine compound and a hydrogen fluoride which evaporate from the reaction system. And optionally a condenser for condensing the desired product which evaporates together.
• the reactor has an element between the still as a reactor and the condenser, for example, a tower-like portion provided on the reactor, for example, a packed tower portion, and converts the fluorine gas into the still gas.
• the perfluoroalkyl iodide which is a reaction raw material, is continuously supplied to the packed portion to allow the reaction to proceed in the packed column portion.
• both the fluorine gas and the perfluoroalkyl iodide may be supplied to the tower-like portion.
• the tower portion may be not only a packed tower type but also a type usually used as a fractionation tower, for example, an old show type, a bubble bell type or a sieve tray type.
• the perfluoroalkyl iodide can be usually supplied as a liquid or a gas.
• Te smell of the invention of course, at the same time IF 5 also generates, therefore, also industrially can be obtained economically.
• Solid-liquid or liquid-liquid separation methods for example, filtration or decantation can be used, and separation and recovery can be carried out as it is by a commonly used fractionation method.
• perfluoroiodoethane is used as the perfluoroalkyl iodide, and octafluorocyclobutane and Z or hydrogen fluoride are used as the perfluoro compound.
• Perfluoroiodoethane is reacted with fluorine gas in the presence of a compound, for example, under reflux conditions to obtain perfluoroethane.
• a reactor having a still and a tower portion provided thereon, and cool the tower portion using, for example, brine.
• IF 5 Since IF 5 is accumulated in the still, may return the remaining liquid to a still therefrom is taken out part still liquid continuously or intermittently to recover the IF 5. Alternatively, until the end of the reaction Accumulate IF 5 to still be recovered IF 5 from the liquid in the still after completion.
• a perfluoroalkyl hexide is used as a perfluoroalkyl iodide to form a perfluoro mouth.
• Xan is generated, and the desired product, perfluorohexane, is used as the perfluoro compound.
• substantially only the perfluorohexane is evaporated by the heat of the reaction, whereby the heat of reaction can be substantially removed.
• only the amount of condensate corresponding to the amount of perfluorohexane supplied to the system (accordingly, corresponding to the amount of hexafluorohexane formed) is used. And return the remainder to the reaction system as reflux.
• this embodiment is carried out in a batch system, the reaction is continued at the full reflux.
• the fluorine gas may be used after being diluted with a gas that is inert to the reaction.
• Nitrogen is an inert gas which can be used, to Liu arm, tetrafurfuryl O b methane, and the like power?, The addition of another component when the separation / removal of components are necessary, the desired product of the present invention, or It may be preferable to use at least one selected from the group consisting of a perfluoro compound, a fluorinated fluoro compound and hydrogen fluoride as a diluent.
• the fluorine gas is diluted in this way, there is an advantage that the fluorine gas can be prevented from being unevenly distributed in the perfluoroalkyl iodide and the contact thereof can be made more uniform.
• the recovered IF 5 was can be used to generate Therefore Pas one Furuoroyo one Doetan the reaction shown below, for example:
• the generated C 2 F 5 I can be used in the reaction (1), and this compound generates various perfluoroalkyl iodides, for example, C 6 F 13 I as shown below.
• FIG. 1 is a schematic flow sheet of an apparatus that can be used in the method of the present invention, and the apparatus used in Examples is substantially the same.
• the illustrated apparatus comprises a reactor 1, a tower section (for example, a packed tower) 2, a condenser 3, and a receiver 4.
• Reactor 1 and Z or tower 2 have a small amount of perfluoro, chlorofluoride, and hydrogen fluoride because reactor 1 and Z or tower 2 have heat generated by the reaction at Z or tower 2 Both compounds are present in the liquid phase and the evaporated compound is cooled by the condenser 3, so that the heat of reaction is removed by such a compound.
• the tower-like portion 2 does not necessarily need to be in the form of a tower, but it is necessary to contact and mix the reactants according to the present invention, and at least one compound selected from a perfluoro compound, a chlorofluoro compound and hydrogen fluoride. Any form may be used as long as the heat removal can be performed.
• Perfluoroalkyl iodide (R f — I) can be supplied via line 5.
• the feed can be performed batchwise or continuously.
• the point to be supplied may be either the reactor 1 or the column 2, and in addition to the line 5 to the liquid phase in the reactor 1, the line 6 to the gas phase of the reactor 1 And at least one of line 7 to tower 2 and the like can be selected.
• the perfluoroalkyl iodide is continuously supplied, the boiling point of the compound having the lowest boiling point among at least one compound selected from the group consisting of a perfluoro compound, a fluorine-containing fluoro compound, and hydrogen fluoride is determined.
• the perfluoroalkyl iodide supplied When the boiling point of the perfluoroalkyl iodide supplied is lower, it is preferable to supply the perfluoroalkyl iodide to the reactor 1. In this case, use line 5 or 6. In addition, at least one selected from a perfluoro compound, a fluoro compound, and hydrogen fluoride When the perfluoroalkyl iodide to be supplied has a higher boiling point than the substance having the highest boiling point among the above compounds, it is preferable to supply the perfluoroalkyl iodide to the tower-shaped portion 2. In this case, use line 7.
• the supply of fluorine gas can be continuously performed to the liquid phase portion of the reactor 1 via the line 8. It is also possible to supply the gas phase of the reactor 1 via the line 9. Further, if necessary, it may be supplied to the tower-shaped portion 2. At least one liquid compound selected from the group consisting of a perfluoro compound, a fluorinated fluoro compound and hydrogen fluoride is supplied to reactors 1 and Z before or simultaneously with the reaction of the perfluoroalkyl iodide with the fluorine gas. Alternatively, it may be supplied to the tower 2. Since these compounds do not participate in the reaction, basically, only a predetermined amount needs to be present in the reaction system unless there is a loss from the reaction system.
• the gas phase vaporized in the reactor 1 and / or the column 2 is introduced via line 10 into the condenser 3 and the condensed liquid is transferred in its entirety or, if necessary, partly via line 11.
• the rest is, for example, the desired compound perfluoroalkane.
• the produced perfluoroalkane R f — F
• This non-condensable gas may be liquefied and recovered in a later processing step, if necessary.
• the liquid in the reactor 1 is removed via an intermittently or continuously line 1 4, generated may be recovered IF 5, or may be processed after ending the reaction.
• the pressure in the reactor can be controlled, for example, by adjusting the opening of the s' valve 15. Can be.
• the presence of at least one liquid selected from the group consisting of a perfluoro compound, a chlorofluoro compound and hydrogen fluoride for example, the presence of ⁇ , ⁇ -fluorocyclobutane, hydrogen fluoride and z or perfluorohexane, etc.
• the reaction heat is efficiently absorbed by contacting a perfluoroalkyl iodide, such as perfluoroethyl iodide or perfluorohexyl iodide, with fluorine gas below and reacting with it, As a result, the reaction temperature can be easily controlled, so that a perfluoroalkane, such as perfluoroethane or hexane, is obtained with high selectivity, and at the same time, iodine pentafluoride is obtained. .
• a perfluoroalkyl iodide such as perfluoroethyl iodide or perfluorohexyl iodide
• a wide-mouth bottle made of fluororesin (PFA) with an internal volume of 500 ml was used as the reactor 1.
• a stopper made of fluororubber was attached to this container, and a hole was made in the rubber stopper to connect the tower portion and the line for supplying raw materials.
• a tube made of SUS 3 16 (outer diameter 6/8 inch, length 100000 mm) was used.
• a cooling jacket was provided at the upper 500 mm part of the SUS tube in the tower-shaped part 2 to form a condenser 3, which was cooled by flowing a refrigerant at 120 ° C.
• the inside of the tower was filled with Hastelloy C mesh.
• the reaction was carried out at normal pressure, during which the liquid in the reactor was in a boiling state, the temperature was constant at 15 ° C, and the reaction was carried out for 7 hours.
• the octafluorocyclobutane evaporating by the reaction heat is cooled / condensed in the column of the condenser 3 to flow down the column, and the non-condensed gas discharged from the top of the condenser 3 is removed.
• Line 13 was extracted (note that in this example, line 10 and line 11 use the same line, and receiver 4 is not used).
• the extracted gas was passed through a mixture of alkali and a reducing agent to absorb and remove the unreacted fluorine gas accompanying the perfluoroethane, and dried and recovered in a calcium chloride tube.
• the obtained gas was analyzed by gas chromatography, the purity of perfluoroethane was more than 99 mol%.
• octafluorocyclobutane was distilled off from the liquid in the reactor to obtain a residue. Analysis of this material, it IF 5 is 9 9 mol% or more was found.
• Example 2 In the same manner as in Example 1, 500 g of octafluorocyclobutane was charged into the reactor and heated to reflux. While stirring the liquid, C 2 F 5 I was supplied via line 5 in the gaseous state at a rate of 6 Ncc / min. Further, fluorine gas diluted to 30 wt% with nitrogen gas was simultaneously supplied to the reactor via the line 8 at a flow rate of 75 Ncc / min.
• Example 3 The reaction was carried out using a device generally called a rectification device.
• Reactor 1 was a still of a rectification column (SUS 3 16 made, 1 L capacity).
• the tower 2 was a rectification column (25 US 200 mm made of SUS316, packed with 20 SUS packing).
• Condenser 3 used a capacitor made of SUS316 (with a heat transfer area of 0.1 m2).
• Reactor 1 was charged with 850 g of hydrofluoric anhydride (hydrogen fluoride), cooled in condenser 3 by flowing a cooling liquid at 120 ° C, and heated while reactor 1 was cooled under atmospheric pressure. Was heated to reflux.
• hydrofluoric anhydride hydrogen fluoride
• fluorine gas (concentration 100%) was charged into the hydrofluoric anhydride liquid phase at a flow rate of 300 Ncc Z min.
• pentafluoroiodoethane (C 2 F 5 I) was introduced into the gas phase of the reactor. ) The gas was charged with 100 Ncc Zmin and reacted.
• the non-condensed gas discharged from the top of the condenser 3 is led from the line 13 to the abatement tower (not shown), washed with a mixed aqueous solution of potassium hydroxide and potassium sulfite, dried, and then subjected to gas chromatography.
• the conversion of pentafluoroiodoethane was 100% and the selectivity of hexafluoroethane was 98.8%.
• Reactor 1 was charged with 107 g of octafluorocyclobutane, and cooled by flowing a cooling liquid at 120 ° C. into condenser 3 while heating reactor 1 to cool octafluorocyclobutane. Orocyclobutane was heated to reflux.
• the pressure in the tower was controlled by controlling the pressure control valve 15 so that the temperature of the still became approximately 1 ° C (gauge pressure 0.4 to 1.5 KG).
• fluorine gas (concentration 100%) is charged into the liquid phase of octafluorocyclobutane at a flow rate of 30 Ncc Zmin, and from line 7, pentafluoroiodoethane (C 2 F 5 I) 10 gas
• the non-condensed gas discharged from the top of the condenser 3 is led from the line 13 to an alkali removal tower (not shown), washed with a mixed aqueous solution of potassium hydroxide and potassium sulfite, and the discharged gas is dried. Chromatographic analysis showed that the conversion of pentafluoroyoethane was 100% and the selectivity of hexafluoroethane was 99.2%.
• Reactor 1 was charged with 860 g of octafluorocyclobutane, and cooled by flowing a cooling liquid at 120 ° C through condenser 3, while reactor 1 was heated, and octafluorocyclobutane was heated under atmospheric pressure. Was heated to reflux.
• Fluorine gas (concentration: 100%) is charged from line 8 into the liquid phase of octafluorocyclobutane at a flow rate of 34 Ncc / min while pentafluoroiodoethane (C 2 F 5 I) gas is supplied from line 7 It was charged at 0 N cc / min.
• the non-condensed gas discharged from the top of the condenser 3 is led from the line 13 to the alkali detoxification tower (not shown), washed with a mixed aqueous solution of potassium hydroxide and potassium sulfite, and the discharged gas is dried. After analysis by gas chromatography, the conversion of pentafluoroiodoethane was 100%. Fluoroethane selectivity was 98.9%. 3 ⁇ 4M116
• a wide-mouth bottle made of fluororesin (PFA) with an internal volume of 750 ml was used.
• a stopper made of fluoro rubber was attached to this container, and a hole was made in rubber ⁇ to connect the tower-like portion.
• a PFA tube (outside diameter 1 inch, length 270 mm) was used, and the inside was filled with a 1/4 inch outside diameter PFA tube cut to about 7 mm.
• Condenser 3 was cooled by flowing a 20 ° C refrigerant using a PFA tube (outside diameter: 1 inch, length: 300 mm) with a jacket.
• a piping joint made of SUS was used for the connection line 11 between the condenser 3 and the tower 2.
• Receiver 4 used a 500 ml PFA bottle and was connected to line 11 via lube 12.
• a perfluoroalkyl iodide preparation line 7 for raw materials was connected to line 11.
• Reactor 1 was charged with perfluorohexane 300, and heated to a total reflux by heating reactor 1 with a water bath. The temperature inside Reactor 1 and inside the tower became 57 ° C. Next, C 6 F13I was charged at 89 mg / min to the top of the column 2 via the line 7. Fluorine gas diluted to 20 wt% with nitrogen was simultaneously introduced into the reactor via the line 9 at a rate of lOONcZmin.
• the reaction was carried out at normal pressure. During this time, the liquid in the reactor was boiling, the temperature was constant at 57 ° C, and the reaction was carried out for 11 hours.
• Residual liquid in the reactor 1 was separated into two layers of IF 5 and C 6 F 14.
• C 6 F 13 is a result of analyzing the contents of the inside of the reactor 1 and the contents of the receiver 4 by gas chromatography, C 6 F 13
• the reaction was carried out using the same apparatus as in Example 6. 100 g of hexane was charged into the reactor 1 and heated to reflux. Raw material C 6 F 13 I was supplied from the top of the column via line 7 at a rate of 92 mg / min. Further, a fluorine gas diluted to 20% with a hexane gas at a perfluoro opening was simultaneously supplied via a line 9 at 100 N cc / min.
• the liquid was cooled / condensed in 3 and all of this liquid was returned to the tower 2 from line 11 (In this example, lines 10 and 11 use the same line, and receiver 4 is not used) T).
• the non-condensable gas discharged from the top of the condenser 3 was extracted from the line 13. Non-condensed gas was absorbed and collected.
• the reaction was carried out at normal pressure. During this time, the liquid in the reactor was in a boiling state, the temperature was constant at 15 ° C, and the reaction was carried out for 5 hours.
• the residual liquid in the reactor 1 was separated into two layers of octafluorocyclobutane in which C 6 F 14 was dissolved and IF 5 .
• the conversion of C 6 F 13 I was 94%, and the selectivity to C 6 F 14 was 95%.

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