Electrochemical acyloxylation of certain aromatic compounds

Claim 2

An electrochemical acyloxylation process comprising subjecting an anhydrous liquid comprising a. an aromatic substrate comprising an aromatic nucleus ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, and b. an anion of strong carboxylic acid having a pK a (H 2 O) at 25 ° C value of less than about 3 to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic substrate wherein an acyloxy group corresponding to said anion replaces said hydrogen.

Claim 3

An electrochemical acyloxylation process comprising subjecting an anhydrous solution comprising a. a molecular aromatic compound ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, and b. an anion of a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3 to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group corresponding to said anion replaces said hydrogen.

Claim 4

An electrochemical acyloxylation process comprising subjecting an anhydrous solution comprising a. a molecular aromatic compound ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, and b. an anion of a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3 to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group corresponding to said anion replaces said hydrogen.

Claim 5

A process according to claim 2 wherein said aromatic compound is selected from the group consisting of aromatic hydrocarbons and aromatic heterocycles.

Claim 6

An electrochemical acyloxylation process comprising subjecting an anhydrous solution comprising a. a molecular aromatic compound ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, b. a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3, and c. a salt of said carboxylic acid to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group selected from the group consisting of said strong carboxylic acid and said salt replaces said hydrogen.

Claim 7

An electrochemical acyloxylation process comprising subjecting an anhydrous solution comprising a. a molecular aromatic compound ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, b. a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3, and c. a salt of said carboxylic acid to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group selected from the group consisting of said strong carboxylic acid and said salt replaces said hydrogen.

Claim 8

A process according to claim 4 wherein said anhydrous solution comprises a carboxylic acid anhydride.

Claim 9

A process according to claim 4 wherein said anhydrous solution comprises a supporting electrolyte.

Claim 10

A process according to claim 4 wherein said strong caboxylic acid has a pK a (H 2 O) at 25° C value of less than 2.

Claim 11

A process according to claim 7 wherein said pk a (H 2 O) at 25° C value is less than 1.

Claim 12

An electrochemical acyloxylation process comprising subjecting an anhydrous solution consisting essentially of a. a molecular aromatic compound ring-substituted with at least one electron-withdrawing moiety, and having at least one replaceable nuclear hydrogen, b. a strong carboxylic acid having a pK a (H 2 O) at 25° C value of about 3, and c. a salt of said carboxylic acid to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group selected from the group consisting of said strong carboxylic acid and said salt replaces said hydrogen.

Claim 13

An electrochemical acyloxylation process comprising subjecting an anhydrous solution consisting essentially of a. a molecular aromatic compound ring-substituted with at least one electron-withdrawing moiety, and having at least one replaceable nuclear hydrogen, b. a strong carboxylic acid having a pK a (H 2 O) at 25° C value of about 3, and c. a salt of said carboxylic acid to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group selected from the group consisting of said strong carboxylic acid and said salt replaces said hydrogen.

Claim 14

A process according to claim 9 wherein said strong carboxylic acid has a pK a (H 2 O) at 25° C value of less than 2.

Claim 15

A process according to claim 10 wherein said strong carboxylic acid has a pK a (H 2 O) at 25° C value of less than 1.

Claim 16

An electrochemical acyloxylation process comprising subjecting an anhydrous solution comprising a. a molecular aromatic compound ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, wherein said moiety is selected from the group consisting of α - haloalkyl, halogenated ethylidene, nitro, nitroso, cyano, carboxyl, carboxylic ester, carboxylic acid anhydride, carbonyl, keto, acyl halide, amido, substituted amido, sulfonium, sulfoxide, sulfone, sulfonate, azo, azoxy, fluoro, chloro, bromo, phosphine oxide, quaternary phosphonium, quaternary ammonium, iodoso, substituted iodoso, iodoxy, chloronium, bromonium, and iodonium, and b. an anion of a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3 to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group corresponding to said anion replaces said hydrogen.

Claim 17

An electrochemical acyloxylation process comprising subjecting an anhydrous solution comprising a. a molecular aromatic compound ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, wherein said moiety is selected from the group consisting of α - haloalkyl, halogenated ethylidene, nitro, nitroso, cyano, carboxyl, carboxylic ester, carboxylic acid anhydride, carbonyl, keto, acyl halide, amido, substituted amido, sulfonium, sulfoxide, sulfone, sulfonate, azo, azoxy, fluoro, chloro, bromo, phosphine oxide, quaternary phosphonium, quaternary ammonium, iodoso, substituted iodoso, iodoxy, chloronium, bromonium, and iodonium, and b. an anion of a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3 to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group corresponding to said anion replaces said hydrogen.

Claim 18

A process according to claim 12 wherein said anion in said an hydrous solution is provided by a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3 and a salt of said acid.

Claim 19

A process according to claim 13 wherein said anhydrous solution comprises a carboxylic acid anhydride and a supporting electrolyte.

Claim 20

A process according to claim 12 wherein said aromatic compound is an aromatic heterocycle.

Claim 21

A process according to Claim 12 wherein said aromatic compound is an aromatic hydrocarbon.

Claim 22

A process according to claim 16 wherein said aromatic hydrocarbon ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen is selected from the group consisting of trifluoromethyl, carbonyl, and carboxylic ester substituted aromatic hydrocarbons.

Claim 23

A process according to claim 17 wherein said aromatic hydrocarbon is benzotrifluoride.

Claim 24

A process according to claim 17 wherein said aromatic hydrocarbon is selected from the group consisting of methyl benzoate and ethyl benzoate.

Claim 25

A process according to claim 17 wherein said aromatic hydrocarbon is benzaldehyde.

Claim 26

A process according to claim 16 wherein said aromatic hydrocarbon ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen is selected from the group consisting of fluoro, chloro, and bromo substituted aromatic hydrocarbons.

Claim 27

A process according to claim 21 wherein said aromatic hydrocarbon is selected from the group consisting of dichlorobenzenes.

Claim 28

A process according to claim 12 wherein said strong carboxylic acid has a pK a (H 2 O) at 25° C value of less than 2.

Claim 29

A process according to claim 23 wherein said pK a (H 2 O) at 25° C is less than 1.

Claim 30

An electrochemical acyloxylation process comprising subjecting an anhydrous solution consisting essentially of a. a molecular aromatic hydrocarbon ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen wherein said moiety is selected from the group consisting of α-haloalkyl, halogenated ethylidene, nitro, nitroso, cyano, carboxyl, carboxylic ester, carboxylic acid anhydride, carbonyl, keto, acyl halide, amido, substituted amido, sulfonium, sulfoxide, sulfone, sulfonate, azo, azoxy, fluoro, chloro, bromo, phosphine oxide, quaternary phosphonium, quaternary ammonium, iodoso, substituted iodoso, iodoxy, chloronium, bromonium, and iodonium, and b. a strong carboxylic acid having a pK a (H 2 O) at 25° C value in the range of 0 to 3, and c. a salt of said strong carboxylic acid to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group selected from the group consisting of said strong carboxylic acid and said salt replaces said hydrogen.

Claim 31

An electrochemical acyloxylation process comprising subjecting an anhydrous solution consisting essentially of a. a molecular aromatic hydrocarbon ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen wherein said moiety is selected from the group consisting of α-haloalkyl, halogenated ethylidene, nitro, nitroso, cyano, carboxyl, carboxylic ester, carboxylic acid anhydride, carbonyl, keto, acyl halide, amido, substituted amido, sulfonium, sulfoxide, sulfone, sulfonate, azo, azoxy, fluoro, chloro, bromo, phosphine oxide, quaternary phosphonium, quaternary ammonium, iodoso, substituted iodoso, iodoxy, chloronium, bromonium, and iodonium, and b. a strong carboxylic acid having a pK a (H 2 O) at 25° C value in the range of 0 to 3, and c. a salt of said strong carboxylic acid to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic compound, wherein an acyloxy group selected from the group consisting of said strong carboxylic acid and said salt replaces said hydrogen.

Claim 32

A process according to claim 25 wherein said aromatic hydrocarbon is selected from the group consisting of trifluoromethyl, chloro, carbonyl, and carboxylic ester substituted aromatic hydrocarbons.

Claim 33

A process according to claim 26 wherein said aromatic hydrocarbon is benzotrifluoride.

Claim 34

A process according to claim 26 wherein said aromatic hydrocarbon is selected from the group consisting of methyl benzoate and ethyl benzoate.

Claim 35

A process according to claim 26 wherein said aromatic hydrocarbon is benzaldehyde.

Claim 36

A process according to claim 26 wherein said aromatic hydrocarbon is selected from the group consisting of dichlorobenzenes.

Claim 37

A process according to claim 26 wherein the pK a (H 2 O) at 25° C value of said strong carboxylic acid is less than 2.

Claim 38

A process according to claim 31 wherein said pK a (H 2 O) at 25° C value is less than 1.

Claim 39

An electrochemical acyloxylation process comprising subjecting an anhydrous liquid consisting essentially of the melt of an organic salt, wherein the cation of said salt comprises an aromatic moiety ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen and wherein the anion of said salt is an anion of a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3, to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic moiety, wherein an acyloxy group corresponding to said anion replaces said hydrogen.

Claim 40

An electrochemical acyloxylation process comprising subjecting an anhydrous liquid consisting essentially of the melt of an organic salt, wherein the cation of said salt comprises an aromatic moiety ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen and wherein the anion of said salt is an anion of a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3, to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic moiety, wherein an acyloxy group corresponding to said anion replaces said hydrogen.

Claim 41

A process according to claim 33 wherein said organic compound is a quaternary ammonium compound and said pK a (H 2 O) at 25° C value is less than 1.

Claim 42

An electrochemical acyloxylation process comprising subjecting an anhydrous liquid consisting essentially of an organic compound selected from the group consisting of quaternary ammonium, quaternary phosphonium, sulfonium, chloronium, bromonium, and iodonium, wherein the cation of said compound contains an aromatic moiety ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, and wherein the anion of said compound is an anion of a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3, to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic moiety wherein an acyloxy group corresponding to said anion replaces said hydrogen.

Claim 43

An electrochemical acyloxylation process comprising subjecting an anhydrous liquid consisting essentially of an organic compound selected from the group consisting of quaternary ammonium, quaternary phosphonium, sulfonium, chloronium, bromonium, and iodonium, wherein the cation of said compound contains an aromatic moiety ring-substituted with at least one electron-withdrawing moiety and having at least one replaceable nuclear hydrogen, and wherein the anion of said compound is an anion of a strong carboxylic acid having a pK a (H 2 O) at 25° C value of less than about 3, to electrolytic conditions sufficient to effect nuclear acyloxylation of said aromatic moiety wherein an acyloxy group corresponding to said anion replaces said hydrogen.