US2700021A

US2700021A - Process for reducing cyclooctatetraene

Info

Publication number: US2700021A
Application number: US196532A
Authority: US
Inventors: Elofson Richard Macleod
Original assignee: General Aniline and Film Corp
Current assignee: GAF Chemicals Corp
Priority date: 1950-11-18
Filing date: 1950-11-18
Publication date: 1955-01-18
Anticipated expiration: 1972-01-18

Description

United States Patent PROCESS FOR REDUCING CYCLO- OCTATETRAENE Richard MacLeod Elofson, Ponoka, Alberta, Canada, as-

signor to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application November 18, 1950, Serial No. 196,532

2 Claims. (Cl. 204-73) This invention relates to a method of reducing cyclooctatriene by electrolytic reduction of cyclooctatetraene.

I have now found that cyclooctratriene can be readily prepared in good yield by electrolytic reduction of cyclooctatetraene. This reduction has been found to take place in neutral and alkaline solutions. However, the present evidence indicates that the reduction does not proceed readily in acidic solutions. The final structure of the cyclooctatriene obtained by electrolytic reduction of cyclooctatetraene has not been definitely established. Some evidence exists that the product of the electrolysis may be a mixture of cyclooctatriene-1,3,5 and cyclooctatriene-1,3,6. However, since the material has drying properties, it appears probable that if the product is considered to be a single substance cyclooctatriene-1,3,6 is formed.

The cyclooctatriene obtained by the process of this invention absorbs 3 moles of hydrogen to form the well known compound cyclooctane. It polymerizes readily with boron trifiuoride and other polymerization catalysts and readily absorbs oxygen to form CsHwOz, the structure of which is unknown at present. It has the comparatively rare property of absorbing oxygen to form a horny resin and as a result is of interest as a substitute for drying oils, such as linseed oil. It is also of interest as a monomer for polymerization reactions and as an intermediate in the synthesis of organic chemicals.

The process of the present invention may most readily be described by consideration of the following specific example thereof:

Example A solution of one hundred grams of tetramethylammonium bromide in one litre of fifty per cent aqueous ethyl alcohol was placed in a two-litre resin pot. The bottom of the still pot was covered with mercury to serve as a cathode to which electrical connection was made. A porous electrolysis cup containing 20% sodium hydroxide as anolyte was suspended in the catholyte media. The anode was a steel rod. To the catholyte was added 100 grams of cyclooctatetraene and the resin pot was covered and fitted with a condenser, to prevent volatiliza tion of cyclooctatetraene and cyclooctatriene, and a stirrer to produce agitation of the two phase system. The electrolysis was now carried out with a current of 68 amperes. After 8 hours the electrolysis was discontinued Patented Jan. 18, 1955 "ice andthe catholyte extracted repeatedly with petroleum ether, P. B. 3560. The ether extracts were dried over NazSOr and fractionally distilled. Cyclooctatriene, P. B. 4647/24 mm., was obtained in 88% yield.

It will be understood that the foregoing .example is illustrative of the invention and that the process embodied in this invention is not limited thereto. As mentioned above, the catholyte media should be neutral to alkaline rather than acidic. It appears that there may be employed as the catholyte any conductive water-organic solvent solution in which cyclooctatetraene is at least partially soluble and which is inert to cyclooctatetraene and cyclooctatriene. Examples of suitable catholyte (mixtures) include low molecular weight organic quaternary compound (tetramethyl ammonium hydroxide, tetramethyl ammonium chloride, tetraethylammonia chlorida, trimethylbenzyl chloride, or mixtures thereof) in the water-organic solvent mixtures. As examples of organic solvents, one may include ethanol, isopropanol, ethylene glycol, dioxane, tetrahydrofurane, ethylene glycol, monomethyl ether and the like. It will also be understood that while mercury was employed as a cathode in the above specific example, other metallic cathodes such as platinum, nickel, copper, iron etc., may be used if desired.

In the above specific example the reduction was carried out at a temperature of about 25 C., and while definite temperature limitations have not been established, it appears that the temperature is not highly critical and temperatures within the range of 0 to C. are operative.

Current densities within the range of 10 to 20 amperes per dm. have been found to be effective. The voltage of the cell is in the range of 10 to 20 volts, depending on the particular catholyte, anolyte and diaphragm.

I claim:

1. The method of producing cyclooctatriene which comprises subjecting cyclooctatetraene to electrolytic reduction in a catholyte which consists of an aqueous lower alkanol containing a lower tetraalkyl ammonium halide at a temperature of 080 C., a current density within the range of 10-20 amperes per dm. and a voltage of 1020 volts.

2. The method of producing cyclooctatriene which comprises subjecting cyclooctatetraene to electrolytic reduction in a catholyte which consists of an aqueous lower alkanol containing a lower tetraalkyl ammonium halide.

References Cited in the file of this patent UNITED STATES PATENTS Adelson et al Jan. 21, 1947 OTHER REFERENCES

Claims

1. THE METHOD OF PRODUCING CYCLOOCTATRIENE WHICH COMPRISES SUBJECTING CYCLOOCTATETRAENE TO ELECTROLYTIC REDUCTION IN A CATHOLYTE WHICH CONSISTS OF AN AQUEOUS LOWER ALKANOL CONTAINING A LOWER TETRAALKYL AMMONIUM HALIDE AT A TEMPERATURE OF 0-80* C., A CURRENT DENSITY WITHIN THE RANGE OF 10-20 AMPERES PER DM.2 AND A VOLTAGE OF 10-20 VOLTS.