USRE23345E - Cyano-substituted tetrahydropyran - Google Patents

Description

Reiuued Feb. 27, 1951 UNITED STATES WANG-SUBSTITUTED TETRAHYDRO PYRAN COIHPOUNDS AND PREPARATION OF THE SAME Curtis W. Smith, Berkeley, Calif., assignor to Shell Development Company, San Francisco, Calm, a corporation of Delaware No Drawing. Original no. 2,489,729, dated November 29, 1949, Serial No. 37,516, July 8, 194:. Application for reissue September 2, 1950,. Se-

rial N0. 183,080

1: Claims. (01. 260-333) Matter enclosed in heavy brackets]: appears in the original patent but nnn no part! this reissue speelflcationf matter printed in italics indicates the additions made I); reissue f This invention relates to new and useful chemical compounds and to a method for their preppounds of the invention in which the tetrahyaration. More'particularly, the invention relates to tetrahydropyranyl alkyl ethers substituted in the heterocyclicnucleus by a cyano'group, e. g.,

6-cyano-2-isobutoxytetrahydropyran, and to a process for the preparation of the novel compounds of the invention.

An object of the invention is new and useful chemical compounds. Another object of the in vention is to provide new and useful chemical compounds by reacting hydrogen cyanide with 2-(3,4-dihydro-1,2-pyranyl) ethers in the presence of a basic condensation catalyst. A further object is new and useful substituted tetrahydropyrans having attached to the heterocyclic nucleus both an alkoxy group and a cyano group, a particular object being such substituted tetrahydropyrans wherein the ether group and the cyano group are bonded to the carbon atoms in the Nos. 2 and 6 positions, respectively, of the heterocyclic ring. A more limited object of the invention is the preparation of new and valuable compounds by reacting 2-(3,4-dihydro-1,2-pyranyl) alkyl others with hydrogen cyanide, in a liquid phase and in the presence of pyridine. Other objects of the invention will become apparent hereinafter.

The foregoing and related objects of the invention have been accomplished by the new chemical 5 compounds hereinafter .described and claimed, and by a method for their preparation, also disclosed and claimed herein. The new compounds to which the invention relates are, broadly stated, monoheterocyclic substituted tetrahydropyrans.- The compounds of the invention are characterized in that there is directly attached to the carbon atom in the No. 6 position of theheterocyclic ring, a cyano group, and in that there is directly linked to the carbon atom in the No. 2

positionoi the heterocyclic ring, an oxygen atom which in tum is directly linked to a hydrocarbon radical of one to eighteen carbon atoms. In the generic concepts or the invention other substitu-' ent groupsmrwatoms'may alsc'be attached to carbon-atoms for the; tetrahydropyran ring; how- .ever,;a preierredf group of compounds consists of in a which the heterocyclic ring, it substituted bylgroups or atoms in addition to the aforesaid cyano group and oxygen atom which is linked dropyran nucleus is disubstituted, i. e., substituted only by the aforesaid essential substituents. L

Generically speaking, the extranuclear oxygen atom which is .directlyattached to the carbon atom in the No. 2 position. of theheterocyclic ring may have its other valency. satisfied by union with any suitable hydrocarbon radicalcontaining from one to eighteen carbon atoms, such as an alkyl, an aryl, a cycloalkyl, -an alkaryl, an aralkyl, or an. unsaturated aliphatic hydrocarbon radical. Representative hydrocarbon radicals 01 from one to eighteen carbon atoms include, among others, methyl, ethyl, 'isopropyl, dodecyl, naphthyl, benzyl, tearyl, cyclohexyi, anthryl, bornyl, phenethy1,-al1yl, methallyl, cyclohexenyl, crotyl, camphanyl, pyrenyl, l-isopentenyl, vinyl cyclohexadienyl, phenyl ethynyl, and iso hexyl. A preferred sub-group of substituted tetrahydropyrans according to the invention are those in which the hydrocarbon group directly linked to said extranuclear oxygen atom is an alkyl group, such as a lower alkyl group, e. g.; containing from one to eight carbon atoms. I

The following are compounds that are illustrative of the invention: 2-isobutoxy-6-cyanotetrahydropyran, 2-methoxy-6-cyanotetrahydropyran, 2-isopropoxy-6-cyanotetrahydropyran, 2-isobutoxy-4-methyl-G-cyanotetrahydropyran, 2-pentoxy-5-methyl6-cyanotetrahydropyran, 2-0ctadecyloxy-4-methyl-6 cyanotetrahydropyran, 2- methoxy-4-phenol 6 cyanotetrahydropyran, 2- octyloxy-G-cyanotetrahydropyran, 2 ethoxy-imethyl 6 cyanotetrahydropyran, 2-allyloxy-6- cyanotetrahydropyran, 2et-hoxy-6-methyl-6-cyanotetrahydropyran, 2-isopropoxy-4 ethyl-6-iiyanotetrahydropyran, 2 hexoxy-fi-cyanotetrahydropyran, 2-vinoxy 6-cyanotetrahydropyran, 2- phenoxy 6 cyanotetrahydropyran, and 2 butoxy-a-methyl-6-cyanotetrahydropyran [and 2- octyloxy-4-phenyltetrahydropyran].

Because 0! the efllcacywith which they may be prepared, and their especially desirable properties,'a preferred subgeneric groupof compounds may be represented-bythe formula in which each R represents hydrogen or lower veniently by reacting dihydropyranyl ethers having the nuclear oleflnic bond in the 5,6 position, with hydrogen cyanide in the presence of a basic condensation catalyst, as in the illustrative specific equations:

Suitable 2 (3,4 dihydro 1,2 pyranyl) alkyl ethers which may be employed as in the above equations for preparation of the present novel compounds, and a method for their preparation, a

are disclosed in the copending application of Smith, Norton, and Ballard, Serial No. 751,980, filed June 2, 1947. Reference is hereby made to said copending application for disclosure of a method for their preparation.

It is essential in accordance with the present invention to conduct the reaction between the dihydropyranyl ether and the hydrogen cyanide in the presence of a basic condensation catalyst. Basic condensation catalysts include broadly those compounds and materials which impart to water, when dissolved therein, a pH value greater than '7. Although any suitable basic condensation catalyst may be used, pyridine is a pflrticularly efllcacious catalyst for the reaction. Other basic condensation catalysts which may be employed include the alkali cyanides; such as NaCN and KCN, inorganic bases, such as KOH, NaOH, Ca(OH) a, C90, LiOH, Ba(OI-I)a, inorganic basic salts, such as NazCOa, NaOOCCI-Ia, NBBPOA, triso dium citrate, CaCOa, Na ethylate, organic bases, such as primary, secondary, and tertiary amines and even quaternary ammonium bases, such as ben zyl trimethyl ammonium hydroxide. An amount of the catalyst within the range of from about 0.2% to 50% of the weight of the reactants is employed, a preferred range being from about 1% to about 10% of the weight of the reactants. The reaction proceeds to good yields of the dey turn from about +50 fective, a preferred range being from about v 4 C. to about 250' C. are ef- C. to about 200 C. The dihydropyranyl ether, the HCN, and the basic condensation catalyst may be mixed in suitable proportions, and the mixture heated as in an autoclave or other closed vessel to maintain the mixture in the liquid state. After a suitable time, generally from about V to 12 hours. the contents of the reaction vessel may be cooled and if desired fractionally distilled or otherwise treated to isolate the cyano-substituted alkoxytetrahydropyran. Isolation of the pure .product, however, is optional, since it frequently may be possible in cases as where the product is to be used in further chemical syntheses, to utilize the crude reaction mixture without isolation of the product.

Dihydropyranyl ethers which may be reacted with HCN according to the invention to form novel and useful cyano-substituted 2-tetrahydropyranyl ethers include the following: 2-(3,4-dihydro-1,2-pyranyl) methyl ether, 2-(3,4-dihydro- 1,2-pyranyl) ethyl ether, 2-(2-methyl-3,4-dihydro-l,2-pyranyl) methyl ether, 2-(6-methyl-3,4- dihydro-lJ-pyranyl) methyl ether, 2-(5-methyl- 3,4-dihydro-l,2-pyranyl) isobutyl ether, 2-(5,6- dimethyl3,4-dihydro-l,2-pyranyl) pentyl ether, 2-(3,4-dihydro-1,2-pyranyl) octyl ether, 2-(4- pentyl-3,4-dihydro-13-Dy anyl) methyl ether, 2- (6-phenyl-3,4-dihydro-1,2-pyranyl) ethyl ether, 2-(3,4-dihydro-1,2-pyranv1) allyl ether, 2-(3,4- dihydro-1,2-pyranyl) vinyl ether, 2-(3,4-dihydro- 1,2-pyranyl) phenyl ether, 2-(3,4-dihydro-l,2- pyranyl) naphthyl ether, and 2-(4-methyl-6-octyl-3,4-dihydro-1,2-pyranvl) phenyl ether.

The following examples will illustrate certain of the preferred embodiments of the invention without, however, being intended to limit the invention as it is defined in the hereto appended claims.

Example I Equimolar amounts of 2-(3,4-dyhydro-1,2-pyranyl) isobutyl ether and hydrogen cyanide were mixed, and to the mixture was added 1% by weight of pyridine. The total mixture was heated in a closed glass-lined reaction vessel at 150 C. for two hours. The mixture was then cooled and fractionally distilled. 2-isobutoxy-6- cyanotetrahydropyran was recovered in a 71% conversion of reactants to product as the fraction distilling at about 73" C. under 0.05-0.07 millemeter mercury pressure. The compound, after one redistillation, was found to have a refractive index ofabout 1.4422 and a specific gravity (20/4) of about 0.979. Analyses for carbon and hydrogen were in good agreement with the theoretical values, as follows: per cent carbon, found 65.7%, calculated for CmHnNOz, 65.5%, per cent hydrogen, found 9.4%. calculated. 9.4%.

Example 11 When the reaction between equimolar amounts of HCN and 2-(3,4-dihydro-1,2-pyranyl) isobutyl ether was conducted in the presence of 2% of pyridine based on the total weight of reactants and at C. for three hours, the conversion of reactants to product was increased to 82% of theory.

The novel compounds of the invention are of value as new and improved chemical intermediates. The position of the cyano group at a saturated carbon atom adJacent to the oxygen atom in the heterocyclic ring imparts unique and unforeseen properties to the products not sed by cyano-substituted tetrahydropyrans in which 5 the cyano group is bonded to a carbon atom other than one which is directly attached to the hetero oxygen atom. The presence at the other carbon atom which is directly united to the oxygen atom in the ring, also accounts tor the improved properties of the products. Acids, esters, and amines may be prepared by hydrolysis, alcoholysis, and reduction. respectively, of the cyano group. Acyclic products may be prepared by treatment with hydrogen in the presence of a hydrogenation catalyst and water, with addition only of the elements of water. The products of the invention include compounds which are useful in themselves as special solvents and blending agents. The novel cyano-substituted alkoxy-tetrahydropyrans have desirable solubility characteristics, andmay be employed. for example, in solvent-extraction procedures. They also include biologi-.

cally active compounds and products useful for the synthesis of biologically active compounds.

I claim as my invention:

1. The substituted tetrahydropyran of the formula INC-I! group of a lower aliphatic monohydric alcohol directly linked to the carbon atom in the No. 2 position of the heterocycle.

4. As a new chemical compound, tetrahydropyran substituted in the No. 6 position by the cyano group and substituted in the No. 2 position by an oxygen atom which is directly linked by its other-valency to a saturated hydrocarbon radical of from three to eight carbon atoms, said tetrahydropyran being otherwise unsubstituted.

5. As a new chemical compound, tetrahydropyran substituted in the No. 6' position by the cyano group and substituted in the No. 2 position by an oxygen atom which is directly linked by its other valency to a hydrocarbon radical of from one to eighteen carbon atoms, said tetrahydropyran being otherwise unsubstituted.

6. As a new chemical compound, a monoheterocyclic, substituted tetrahydropyran characterized in that there is a cyano group directly linked to the carbon atom in the No. [2] 6 position of the heterocycle and additionally characterized in that there is directly linked to the carbon atom in the No. 2 position of the heterocycle an oxygen atom which in turn is directly attached to a hydrocarbon group of from one to eighteen'carbon atoms.

I. A process for the preparation of 6-cyano-2- isobutoxytetrahydropyran which comprises reacting at a temperature within the range of from about 50 C. to about 250 C. 2-(3,4-dihydro-l,2- pyranyl) isobutyl ether with hydrogen cyanide in the presence of pyridine. r

8. A process for the preparation of 6-cyano-2- isobutoxytetrahydropyran which comprises mixing 2-(3,4-dihydro-1.2-Dyranyl) isobutyl ether and an. about equirnolar amount of'hydrogen cyanide and heating the mixture in the liquid state in the presence of pyridine at about 150 C. for about 3 hours.

9. A process for the preparation of 6-cyano-2- isobutoxytetrahydropyran which comprises reacting at a temperature within the range of from about 50 C. to about 250 C. 2-(3,4-dih ydro-1,2- pyranyl) isobutyl ether with hydrogen cyanide in a liquid phase in the presence of a basic condensation catalyst.

10. A process for the preparation of tetrahydropyran substituted in the No. 6 position by the cyano group and in the No. 2 position by an alkoxy group which comprises reacting a 2-dihydropyranyl alkyl ether having the nuclear oleflnic bondin the 5,6-position of the nucleus withhydrog'en cyanide in a liquid phase in the presence of pyridine at a temperature within the range of from about 100 C. to about 200 C.

11. A process for the preparation of tetrahy- .dropyran substituted in the No. 6 position by the cyano group and in the No. 2 position by an alkoxy group which comprises reacting at a temperature within the range of from about 50 C. to about 250 C. a 2-dihydropyranyl alkyl ether with hydrogen cyanide in the presence of a basic condensation catalyst.

12. A process for the preparation of a cyanosubstituted 2-tetrahydropyranyl organicether by prises reacting hydrogen cyanide with anorganic oxy-ether of a 3,4-dihydro-L2-pyran-2-ol by heating a reaction mixture thereof in the presence of a basic condensation catalyst at a temperature within the range of from about 50 C. to about 250 C.

. CURTIS W. SMITH.

No references cited.