US2833831A

US2833831A - Preparation of perfluorodienes

Info

Publication number: US2833831A
Application number: US522177A
Authority: US
Inventors: Haszeldine Robert Neville
Original assignee: Individual
Current assignee: Individual
Priority date: 1954-07-26
Filing date: 1955-07-14
Publication date: 1958-05-06
Anticipated expiration: 1975-05-06

Description

United States Patent@ 2,835,831 PREPARATION or PERFLUORODIENES Robert Neville Haszeldine, Cambridge, England No Drawing. Application July 14, 1955 Serial No. 522,177

Claims priority, application Great Britain July 26, 1954 9 Claims. or. 260-4533) This invention is concerned with polyfiuorinated organic compounds; more particularly, but not exclusively, this invention is concerned with conjugated and uncon ugated perfluorodienes and certain derivatives of such compounds.

U. S, specification No. 2,668,864 discloses the preparation of terminally unsaturated aliphatic perfluoro monoolefins by a dry reaction which is conveniently carried outat'atmospheric pressure and which involves the pyro lytic vdecarboxylation and defiuorination of an anhydrous 1 alkali metal salt of a perfiuoro-alkyl monocarboxylic acid. It isstated in this U. S. specification that the ob-' taining' of high yields of fluorocarbon olefins from this reaction is peculiar to the salts of monocarboxylicacids .and that salts of; polycarboxylic acids do not produce per- In accordance with a firstaspectof this invention, it has 7 beendiscovered that the above pyrolysis reaction can, in fact, be applied to the'dialkali metal salts of perfluoroalkyl dicarboxylic acids to produce satisfactoryyields of "tion would, by reason of the two double .bonds therein, be

too reactive and unstable to permit of satisfactory yields. This is particularly the case Where theproduct theoretically obtainable from the pyrolysis reaction is aconjugated diene, since a compound of this type is far more reactive than, and exhibits properties markedly different from, a non-conjugated diene and might thus have been expected to undergo side reactions and/ or complete breakdown; thus, for example, the compound hexafluorobutadiene-l,3, the theoretical productof the pyrolysis of a dialkali metal salt of octafluoroadipic acid, is extremely reactive and yields dimers and'trimers when subjected to elevated temperatures at atmospheric pressure. The pyrolysis reaction is thereforeof particular interest in its application to thepreparation of conjugated dienes, notably the useful diene hexafluorobutadiene-l,3.

More specifically, this firstaspect of the invention may be stated to reside in subjecting to pyrolysis, at a subatmospheric pressure, an anhydrous compound having the formula:

in-which M is an alkali metal; preferably sodium, and n isan integer of at least 4, preferably an integer from 4 to 20 or 24 'or'so. The diene recovered from the pyrolysis has two carbon atoms less than its precursor and has the formula:

in which m=rt-4, so that, when n=4 to 20, m is zero or an integer from 1 to 16. t

I 2,833,831 T P atented 6, 1958 In the pyrolysis of the dialkali metal salts; the salts must be anhydrous and are desirably spread in a thin layer upon an inertsupporting material such asplatinum foil, for example, and placed in a furnace tube constructed of some inert material, such as nickel. An inert reaction vessel is necessary in order to prevent reaction. thereof with gaseous productsat the high temperatures of pyrolysis. The furnace is in general evacuated toa pressure of below 300 mm. and preferably l0 to 20 mm., of mercury absolute and is heated rapidly to a temperature in the range of 100 to 450 C. Preferably the temperature is raised rapidly to that'atwhichreaction begins. The time of reaction may be between 0.1 and 10 hours depending upon thereaction' temperature.

The volatile productsof the reaction are collected in traps cooled to a low temperature by a medium such as liquid oxygen, for example, and are then transferred to a distillation system where they are separated into fractions. Exemplary of the dialkali metal salts of perfluoro dicarboxylic acids: which may be pyrolyzed according to the process of the invention are Na0 C( CF CO Na,

Particularly when the above-described pyrolysis of dialkali metal salts of perfluoro-alkyl dicarboxylic acids is carried out under relatively mild conditions, there may be formed, asa by-product, the acyl fluoride of a perfluoroalkly monocarboxylic acid having a terminal olefinic bond 'Which may likewise be subjected to-pyrolysis at subatmospheric pressures to produce satisfactory yields of dienes which again may be either conjugated or unconjugated. This reaction, which constitutes a second aspect of this invention, is also surprising in view of the greater reactivity of the mono-olefinic starting material as compared with a corresponding fully saturated material as employed in the U. S; specification cited above, and also of course for reasons similar to those advanced above in' connection with the pyrolysis of the dicarboxylic acid salts;

r In accordaucetherefore with this second aspect of the invention, thereis subjected to pyrolysis, at sub-atmos pheric pressures, an anhydrous compound having the formula:

in which M is an alkali metal, preferably sodium, and n is an integer of at least 2, preferably an integer from 2 to 18. The dienes recovered as products of this process possess one less carbon atom than their precursors and have the formula:

Q "F C=CF(CF ),,,CF=CF in which m=n2, sothat m has a value from zero to 16 when 12:2 to 18. -When in the above formulae 11:2 and m=0, the invention provides a novel route to theuseful conjugated diene perfluorobutadiene-l,3. In the pyrolysis of the alkali metal salts .of unsaturate perfluoro" monocarboxylic acids, the salt is powdered,

thoroughly dried and pyrolyzed on a platinum-"or other inert support placed in an evacuated nickel furnace tube in a manner similar to that described above in'connection with the pyrolysis of dialkali metal salts of saturated perfluoro dicarboxylic acids. The pyrolysis may be effected at atemperature in the range of to 450- C. during a period of 0.1 to 10 hours depending upon the reaction temperature. The volatile products are separated by distillation. Exemplary of the salts of unsatu-- Although unsaturated perfiuoro monocarboxylic acids may be produced, as mentioned above, from the by-prodnets of the pyrolysis of dialkali metal salts of saturated perfiuoro dicarbooxylic acids, it is to be understood that these compounds can be prepared in other ways for use in the invention.

In. both the above reactions involving alkali metal salts of perfluoro carboxylic acids, the sodium salts are preferred for reasons of cheapness, but it is to be understood that lithium, potassium, rubidium and cesium salts are also usable.

The alkali metal salts of unsaturated perfluoro monocarboxylic acids used in the pyrolysis reaction just described, or the free acids themselves, may be converted to the corresponding silver salts which on reaction with iodine, bromine or chlorine undergo decarboxylation to yield a polyfluoro halogenoalkene and/or a polyfluorohalogenoalkane. These reactions which, it may be noted, are quite generally applicable to silver salts of the formula CF =CF(CF ),,COOAg where n is an integer of l or more, may be represented as follows:

Inorganic where M is an alkali metal or hydrogen, and n is an integer of 1 or more, preferably not more than 20.

when X=Cl or Br.

Although it is known (vide, Haszeldine, J. Chem. Soc. 4259, 1952) that the silver salts of perfluoroalkyl monocarboxylic acids undergo decarboxylation with halogens to form the corresponding halides, it was surprising to find that the reaction also proceeds and gives high yields with the silver salts of unsaturated perfluoro monocarboxylic acids.

As an example of the silver salt reaction with halogen, silver perfluoro-4-pentenoate (prepared by treating perfluoro-4-pentenoic acid with an inorganic silver salt) may be caused to react with iodine to form 4-iodo-perfluorobutene-l, which latter compound may in turn be caused to react with chlorine or bromine to form 1,2,4-trichloroor -bromo-heptafluorobutane.

Reactions (1) and (2) indicated above are of particular interest in that they yield new classes of compounds. Reaction (1) yields new compounds of the formula F C=CF(CF ),,CO Ag, where n is an integer preferably from 1 to 20; and reaction (2) yields new iodo compounds of the formula F (,'CF(CF ),,I where n is an integer of at least 2, preferably 2 to 20, and also new compounds of the formula CF XCFX(CF ),,X where n is an integer of at least 2, preferably 2 to 10, and X is chlorine or bromine.

Although the silver salt/halogen reaction is set forth above as applying to unsaturated silver salts of the formula F C= CF(CF ),,CO Ag, where n is an integer of 1 or more, it is to be noted that the reaction also surprisingly proceeds between iodine and the compound "F C=CFCO Ag to produce the compound CF =CFL The invention will be further illustrated by reference to the following specific examples in which all parts are by weight:

Example 1 Octafluoroadipic acid was prepared by one of the routes reported in the literature, namely by the oxidation of perfluorocyclohexene (Haszeldine, Nature 168, 1028, 1951), and was converted into the disodium salt by neutralization with aqueous sodium hydroxide. The salt, isolated by evaporation of the aqueous solution to dryness in vacuo, was ground in a mortar and thoroughly dried at a temperature of 120 C. in vacuo.

Five parts of the anhydrous disodium octafluoroadipate were spread in a thin layer in a horizontal open cylinder of platinum foil, which was then inserted into a horizontal nickel furnace tube having an internal diameter of one inch. The furnace tube was sealed at one end and evacuated to a pressure of 10" mm. Two glass traps cooled by liquid oxygen were connected in series between the furnace tubes and the vacuum pump. The furnace was I then heated stepwise to a temperature of 450 C. during a period of 2.5 hours, the traps being periodically examined during the heating. No reaction was detected at a furnace temperature up to and including 200 C., but appreciable reaction occurred when a temperature of 300 C. was attained, and there was little sign of further reaction at temperatures above 370" C. The combined volatile products were transferred to a vacuum system where they were separated into fractions boiling above or below a temperature of 10 C.

Infra-red spectroscopic examination of the more volatile fraction showed it to contain hexafluorobutadiene- 1,3, contaminated by carbon dioxide and by material (probably acyl fluorides) which showed carbonyl absorption at 5.3 This fraction was then washed with 2 N aqueous sodium hydroxide and distilled to yield 0.73 part of hexafluorobutadiene-L3, a yield of 30 percent, boiling point 5.7 C. (Found: C, 29.7; M, 162. Calculated for C 1 C, 29.6; M, 162.) The boiling point and infrared spectrum of the purified material were identical with those reported earlier (Haszeldine, J. Chem. Soc. 4423, 1952). Repetitions of this experiment produced yields of hexafiuorobutadiene of 32, 37 and 25 percent by weight.

Infra-red spectroscopic examination of the less volatile fraction (M, 240) showed it to contain the CF COF group C=O absorption at 5.31m cf. CF COF 5.25m C F COF. 5.29 cf. CF CF=CF 556 C F CF=CF= 5.56 see J. Chem. Soc. 4423, 4259, 1952). The fraction was shaken with 5 parts of water in a sealed tube and the primary portion of the fraction dissolved, leaving 0.05 part of an unidentified fraction, boiling point C. (isoteniscope) (M, 275). The aqueous solution, which gave a positive test for fluoride, was extracted ten times with a total of 2.1 parts of ether. The ethereal solution was dried over sodium sulfate and, after removal of the ether, the residual liquid was distilled from a small amount of phosphoric anhydride through a short column and 0.69 part of perfluoro-4-pentenoic acid was recovered, equivalent to a yield of 21 percent by weight, boiling point 75 to"76 C./59 mm. Hg absolute. (Found: C, 26.4; H, 0.5; equivalent 226. C H0 F requires C, 26.6; H, 0.4; equivalent 226.) The infra-red spectrum of the acid showed a band at 5.62 revealing the presence of a carboxyl group; the C=C stretching absorption is combined with this band.

Examination of the solid residue from the pyrolysis of sodium octafluoroadipate showed it to contain sodium fluoride, carbon and carbonaceous material.

Example 2 1.02 parts of perfluoro-4-pentencic acid were neutralized with 5 N aqueous sodium hydroxide and the anhydrous sodium salt was obtained by evaporation of the aqueous solution in vacuo. Thesalt was powdered, re-

dried at a temperature of 120C. and-a pressure of mm. Hg absolute, and then placed in the platinum cylinder and furnace described in Example 1 above. The pyrolysis of the salt was accomplished by raising the temperature of the furnace from 160 to 450 C. over a period of 2.5 hours. The residual sodium fluoride contained only a small amount of carbon. The volatile products were shaken in a sealed tube with 2 N aqueous sodium hydroxide and then distilled to yield 61 percent by weight of hexafiuorobutadiene-1,3 identified by comparison of its infra-red spectrum with that recorded in J. Chem. Soc. 4423, 1952. When mixed with a slight excess of chlorine and exposed to ultra-violet light,-two molecules of chlorine were absorbed to give 1,2,3,4-tetrachlorohexafiuorobutane identical with the compound described in J. Chem. Soc. 4423, 1952.

Example 3 1.2 parts of perfiuoro-4-pentenoic acid were dissolved in water and treated with a slight excess of freshly prepared silver carbonate and a 97 percent yield of silver perfluoro-4-pentenoate was obtained. (Found: Ag, 32.3. C O F Ag requires Ag, 32.4.) The product was isolated as a white crystalline solid by evaporation of the aqueous solution to dryness in vacuo.

Example 4 1.5 parts of silver perfluoro-4-pentenoate were mixed with a 300 percent excess of dry, finely powdered iodine in a silica flask connected to two traps cooled by liquid oxygen. The pressure in the apparatus was maintained at 300 mm. Hg absolute and the solid mixture was heated by means of a small flame. A smooth reaction occurred, and, after pumping the evolved gases into the traps, the combined volatile material was washed in a sealed tube with aqueous sodium hydroxide. The residual organic material was purified by distillation in vacuo to provide a 72 percent by weight yield of 4-iodoperfluorobutene-1, boiling point (isoteniscope) 20 C./ 65 mm. Hg absolute, ca. 70 C./760 mm. Hg absolute (micro). (Found: C, 15.4; M, 309. C IF requires C, 15.6; M, 308.) The compound shows a band at 5.58 1 in the infra-red.

. Example 5 0.7 part of 4-iodoperfluorobutene-1 was treated with an excess of chlorine in a sealed silica tube exposed to ultraviolet light for two days to produce an 83 percent by weight yield of 1,2,4-trichloroheptafiuorobutane, boiling point 96 to 97 C. (micro). (Found: C, 16.8; M, 285. C CI F requires C, 16.7; M, 287.5.)

The same compound was obtained by reaction of an excess of dry chlorine with a silver heptafluoropentenoate in a sealed tube at a temperature of 100 C.

The new silver salts provided by this invention are useful for the preparation of esters and auhydrides as illustrated by the following reactions:

where M=hydrogen, alkyl, aryl or metal, and X=halogen.

stituted" aryl, halogen or'a suitable functional group; Thenewsilver-salts may also be used for the preparation of fire extinguishing media, as illustrated byreaction (3) below, and for thepreparation of unsaturated compounds which are in turn useful in the preparation of plasticisers and polymers as illustrated by reaction (4) below:

The new iodo compounds provided by this invention are useful for the preparation of dienes as illustrated by reaction (1) below and are also particularly useful for the preparation of coupled products as described in my copending application No. 377,716, filed August 31, 1953, v

and as illustrated by reaction (2) below.

CFFCF(CF2)2I CHFCHF dehydro- I claim:

1. A process for the preparation of a perfiuorodiene which comprises subjecting to pyrolysis, at a pressure below about 300 mm. of mercury absolute, an anhydrous compound having the formula in which M represents an alkali metal and n is aninteger from 4 to 20, thereby producing a perfluorodiene having two less carbon atoms than its precursor and having the formula I a pressure below about 300 mm. of mercury absolute.

6. A process according to claim 1, wherein the pyrolysis is carried out under relatively mild conditions where- 'by there is formed as by-product a compound of the formula:

F C=CF(CF ),,CO M

where M represents an alkali metal and n an integer from 2 to 18.

7. A process for the preparation of a perfluorodiene which comprises subjecting to pyrolysis, at a pressure below about 300 mm. of mercury absolute, an anhydrous compound having the formula:

in which M is an alkali metal radical and n is an integer from 2 to 18, thereby producing a perfluorodiene having one less carbon atom than its precursor and having the formula:

in which m has a value from zero to sixteen.

2,sse,se1

7 S 8. A process according to claim 7, in which M in the and at a temperature between about 100 C. and about formula of the starting material represents sodium. 450 C. to produce a diene having the formula 9. A process for the preparation of a perfluorodiene which comprises subjecting to pyrolysis at a pressure F2C=CF(CFZ)" 4CF=CF2 below about 309 mm. of mercury absolute, an anhydrous 5 References Cited in the fil f this Patent compound having the formula UNITED STATES PATENTS 2 2)n 2,176,181 Hunsdiecker Oct. 17, 1939 in which M represents an alkali metal and n is an integer 260L536 Zane June 1952 from 4 to 20 to form a compound having the formula 10 2647933 La Zerte et 1953 2,668,864 Hals et a]. Feb. 9, 1954 F C cF(CF CO M 2,678,953 Conly May 18, 1954 2,689,251 Hamilton et al Sept. 14, 1954 and then further heating the last identified compound, at 2,704,776 La Zerte et a1 Feb. 24, 1955 a pressure below about 300 mm. of mercury absolute 15 2,716,668 Haszeldine Aug. 30, 1955 UNITED STATES PATENT OFFICE Certificate of Correction Patent N 0. 2,833,831 May 6, 1958 Robert Neville Haszeldine It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.

Column 3, lines 5 and 7, for that portion of the formula reading (OF each occurrence, read (CF line 12, for dicarbooxylic read dicarboxy1ic; line 39, for when X=1 read When X=I; line 43, the formula should appear as shown below instead of as in the patent:

orzxorxwronx column 5, line 64, Formula 2, the right-hand portion should appear as shown below instead of as in the patent:

[OF =CF(OF2)1,CO]2O column 6, line 27, for that portion of the first formula reading CF= OF (GF CH GHFI read CF CF (CF OH CHFI Signed and sealed this 19th day of August 1958.

fittest: KARL H. AXLINE, ROBERT C. WATSON, Attestz'ng Oficer. Gammz'ssioner of Patents.

Claims

1. A PROCESS FOR THE PREPARTAION OF A PREFLUORODIENE WHICH COMPRISES SUBJECTTING TO PYROLYSIS, AT A PRESSURE BELOW ABOUT 300 MM. OF MERCURY ABSOLUTE, AN ANHYDROUS COMPOUND HAVING THE FORMULA