Oxidation of monohydroxy aryl compounds to 1,4-quinones

Claim 2

A process for preparing 1,4-benzoquinones or naphthoquinones comprising contacting a monohydroxy aryl compound unsubstituted in the position para to the hydroxyl group and selected from the group consisting of phenol, α-naphthol, and mono- and dialkyl phenols and α-naphthols, in solution in a nitrile containing a copper salt with an oxygen-containing gas at a temperature in the range of about from 0° to 100° C. and under an oxygen partial pressure of about from 7 to 200 atmospheres, said phenol, α-naphthol, or mono- or dialkyl phenol or α-naphthol optionally being alkoxysubstituted and the alkyl substituents in said mono- or dialkyl phenol or α-naphthol containing 1 to 12 carbon atoms, said nitrile and said copper salt together forming a complex which is soluble in the reaction system, and said copper salt being selected from the group consisting of cuprous chloride, cupric chloride, cuprous bromide, cupric bromide, cupric nitrate, and cupric acetate with the proviso that a source of chloride or bromide ion is present when said copper salt is cupric acetate.

Claim 3

A process of claim 1 wherein said monohydroxy aryl compound is an o- or m-alkyl phenol and said oxygen partial pressure is at least about 14 atmospheres.

Claim 4

A process for preparing 1,4-benzoquinones or naphthoquinones comprising contacting a monohydroxy aryl compound unsubstituted in the position para to the hydroxyl group and selected from the group consisting of phenol, α-naphthol, and mono- and dialkyl phenols and α-naphthols, in solution in a nitrile containing a copper salt with an oxygen-containing gas at a temperature in the range of about from 0° to 100° C. and under an oxygen partial pressure of about from 7 to 200 atmospheres, said phenol, α-naphthol, or mono- or dialkyl phenol or α-naphthol optionally being alkoxysubstituted and the alkyl substituents in said mono- or dialkyl phenol or α-naphthol containing 1 to 12 carbon atoms, said nitrile being selected from the group consisting of acetonitrile, propionitrile, butyronitrile, adiponitrile, glutaronitrile, 2-methylglutaronitrile, benzonitrile, and tolunitrile, and said copper salt being selected from the group consisting of cuprous chloride, cupric chloride, cuprous bromide, cupric bromide, cupric nitrate, and cupric acetate, with the proviso that a source of chloride or bromide ion is present when said copper salt is cupric acetate.

Claim 5

A process for preparing 1,4-benzoquinones or naphthoquinones comprising contacting a monohydroxy aryl compound unsubstituted in the position para to the hydroxyl group and selected from the group consisting of phenol, α-naphthol, and mono- and dialkyl phenols and α-naphthols, in solution in a nitrile containing a copper salt with an oxygen-containing gas at a temperature in the range of about from 0° to 100° C. and under an oxygen partial pressure of about from 7 to 200 atmospheres, said phenol, α-naphthol, or mono- or dialkyl phenol or α-naphthol optionally being alkoxysubstituted and the alkyl substituents in said mono- or dialkyl phenol or α-naphthol containing 1 to 12 carbon atoms, said nitrile being selected from the group consisting of acetonitrile, propionitrile, butyronitrile, adiponitrile, glutaronitrile, 2-methylglutaronitrile, benzonitrile, and tolunitrile, and said copper salt being selected from the group consisting of cuprous chloride, cupric chloride, cuprous bromide, cupric bromide, cupric nitrate, and cupric acetate, with the proviso that a source of chloride or bromide ion is present when said copper salt is cupric acetate.

Claim 6

A process of claim 3 wherein said monohydroxy aryl compound is selected from the group consisting of phenol, o-alkyl phenols, and m-alkyl phenols.

Claim 7

A process of claim 3 wherein said solution of monohydroxy aryl compound is contacted with said oxygen-containing gas in a continuous manner, and said temperature is in the range of about from 5° to 40° C.

Claim 8

A process of claim 5 wherein said oxygen-containing gas is air.

Claim 9

A process of claim 3 wherein said monohydroxy aryl compound is contacted with said oxygen-containing gas at a temperature in the range of about from 20° to 75° C. and under an oxygen partial pressure of about from 14 to 100 atmospheres.

Claim 10

A process of claim 7 wherein the molar ratio of said monohydroxy aryl compound to said copper salt is in the range of about from 5/1 to 25/1.

Claim 11

A process of claim 7 wherein up to about 50 percent by volume of water is present in the nitrile solution, based on the total volume of solution.

Claim 12

A process for preparing p-benzoquinone comprising contacting phenol in solution in a nitrile containing a copper salt with an oxygen-containing gas at a temperature in the range of about from 0° to 100 ° C. and under an oxygen partial pressure of about from 20 to 200 atmospheres, said nitrile and said copper salt together forming a complex which is soluble in the reaction system, said copper salt being selected from the group consisting of cuprous chloride, cupric chloride, cuprous bromide, cupric bromide, cupric nitrate, and cupric acetate with the proviso that a source of chloride or bromide ion is present when said copper salt is cupric acetate.

Claim 13

A process for preparing p-benzoquinone comprising contacting phenol in solution in a nitrile containing a copper salt with an oxygen-containing gas at a temperature in the range of about from 0° to 100 ° C. and under an oxygen partial pressure of about from 20 to 200 atmospheres, said nitrile and said copper salt together forming a complex which is soluble in the reaction system, said copper salt being selected from the group consisting of cuprous chloride, cupric chloride, cuprous bromide, cupric bromide, cupric nitrate, and cupric acetate with the proviso that a source of chloride or bromide ion is present when said copper salt is cupric acetate.

Claim 14

A process of claim 10 wherein said nitrile is selected from the group consisting of acetonitrile, adiponitrile, and benzonitrile.

Claim 15

A process of claim 11 wherein said phenol is contacted with said oxygen-containing gas at a temperature in the range of about from 20° to 75° C., and the molar ratio of phenol to said copper salt is in the range of about from 5/1 to 25/1.

Claim 16

A process of claim 1 wherein said monohydroxy aryl compound is a dialkyl phenol.

Claim 17

A process of claim 13 wherein the alkyl substituents in said dialkyl phenol are methyl groups.

Claim 18

A process of claim 14 wherein said dialkyl phenol is 2,6-dimethylphenol.

Claim 19

A process of claim 14 wherein said dialkyl phenol is 3,5-dimethylphenol.