Regiospecific aryl nitration of meso-substituted tetraarylporphyrins

Claim 2

A process for the direct nitration of a tetraarylporphyrin compound comprising contacting a tetraarylporphyrin compound of the formula ##STR7## or a metallo derivative thereof wherein each X represents an aryl moiety each of which is unsubstituted or independently substituted with up to four same or different substituents selected from the group consisting of aryl, alkyl, halo, alkylaryl, alkoxy, or carboalkoxy with a molar excess of from about 10:1 to about 300:1 of a nitrating agent in a suitable solvent in the presence of an amount of sulfuric acid that is less than equimolar relative to the amount of nitrating agent under conditions such that at least one peripheral aryl moiety is nitrated.

Claim 3

The process of claim 1 wherein the nitrating agent is nitric acid having a specific gravity of between about 1.4 and about 1.6.

Claim 4

The process of claim 1 wherein the nitrating agent is nitric acid having a specific gravity of about 1.6.

Claim 5

The process of claim 1 wherein the suitable solvent is selected from the group consisting of acetic acid, methylene chloride, and chloroform.

Claim 6

The process of claim 1 wherein the suitable solvent is chloroform.

Claim 7

The process of claim 1 wherein at least about 20% of the theoretical maximum of desired product is formed.

Claim 8

The process of claim 1 wherein at least about 50% of the theoretical maximum of desired product is formed.

Claim 9

The process of claim 1 wherein the tetraarylporphyrin compound is mono-nitrated.

Claim 10

The process of claim 1 carried out in the absence of sulfuric acid.

Claim 11

The process of claim 1 carried out in the substantial absence of sulfuric acid.

Claim 12

The process of claim 1 carried out at a temperature of from about -10° C. to about 25° C. and at about atmospheric pressure.

Claim 13

The process of claim 1 carried out in an inert atmosphere.

Claim 14

The process of claim 1 wherein the ratio of nitrating agent:tetraarylporphyrin compound is from about 10 to about 32:1.

Claim 15

The process of claim 1 wherein said tetraarylporphyrin compound is selected from the group consisting of tetraphenylporphyrin, tetratolylporphyrin, tetramesitylporphyrin, tetranaphthylporphyrin, tetra-3-chlorophenylporphyrin, tetra-3-methoxyphenylporphyrin, and tetraanthracenylporphyrin.

Claim 16

The process of claim 1 wherein the substituents on the aryl moiety are selected from the group consisting of alkyl of one to four carbon atoms, phenyl, naphthyl, bromo, chloro, and methoxy.

Claim 17

A process for the direct nitration of a tetraarylporphyrin compound comprising contacting a tetraarylporphyrin compound of the formula ##STR8## wherein each R independently represents hydrogen, aryl, alkyl, halo, alkylaryl, alkoxy, or carboalkoxy with a molar excess of from about 10:1 to about 300:1 of nitric acid in a suitable solvent in the presence of an amount of sulfuric acid that is less than equimolar relative to the amount of nitric acid under conditions such that at least one peripheral aryl moiety is nitrated at the para position.

Claim 18

A process for the direct nitration of a tetraarylporphyrin compound comprising contacting a tetraarylporphyrin compound of the formula ##STR8## wherein each R independently represents hydrogen, aryl, alkyl, halo, alkylaryl, alkoxy, or carboalkoxy with a molar excess of from about 10:1 to about 300:1 of nitric acid in a suitable solvent in the presence of an amount of sulfuric acid that is less than equimolar relative to the amount of nitric acid under conditions such that at least one peripheral aryl moiety is nitrated at the para position.

Claim 19

The process of claim 16 wherein the nitrating agent is nitric acid having a specific gravity of between about 1.4 and about 1.6.

Claim 20

The process of claim 16 wherein the nitrating agent is nitric acid having a specific gravity of about 1.6.

Claim 21

The process of claim 16 wherein the suitable solvent is selected from the group consisting of acetic acid, methylene chloride, and chloroform.

Claim 22

The process of claim 16 wherein the suitable solvent is chloroform.

Claim 23

The process of claim 16 wherein at least about 20% of the theoretical maximum of desired product is formed.

Claim 24

The process of claim 16 wherein at least about 50% of the theoretical maximum of desired product is formed.

Claim 25

The process of claim 16 wherein the tetraarylporphyrin compound is mono-nitrated.

Claim 26

The process of claim 16 carried out in the absence of sulfuric acid.

Claim 27

The process of claim 16 carried out in the substantial absence of sulfuric acid.

Claim 28

The process of claim 16 carried out at a temperature of from about -10° C. to about 25° C. and at about atmospheric pressure.

Claim 29

The process of claim 16 carried out in an inert atmosphere.

Claim 30

The process of claim 16 wherein the ratio of nitrating agent:tetraarylporphyrin compound is from about 10 to about 32:1.

Claim 31

The process of claim 16 wherein said tetraarylporphyrin compound is selected from the group consisting of tetraphenylporphyrin, tetratolylporphyrin, tetra-3-chlorophenylporphyrin, tetra-3-methoxyphenylporphyrin, and tetramesitylporphyrin.

Claim 32

The process of claim 16 wherein the substituents on the aryl moiety are selected from the group consisting of alkyl of one to four carbon atoms, phenyl, naphthyl, bromo, chloro, and methoxy.

Claim 33

A process for preparing an amino tetraarylporphyrin which comprises contacting a tetraarylporphyrin compound of the formula ##STR9## or a metallo derivative thereof wherein each X represents an aryl moiety each of which is unsubstituted or independently substituted with up to four same or different substituents selected from the group consisting of aryl, alkyl, halo, alkylaryl, alkoxy, or carboalkoxy with a molar excess of from about 10:1 to about 300:1 of a nitrating agent in a suitable solvent in the presence of an amount of sulfuric acid that is less than equimolar relative to the amount of nitrating agent under conditions such that at least one pripheral aryl moiety is nitrated; and reducing the nitrated tetraarylporphyrin to its amino derivative.

Claim 34

A process for preparing an amino tetraarylporphyrin which comprises contacting a tetraarylporphyrin compound of the formula ##STR9## or a metallo derivative thereof wherein each X represents an aryl moiety each of which is unsubstituted or independently substituted with up to four same or different substituents selected from the group consisting of aryl, alkyl, halo, alkylaryl, alkoxy, or carboalkoxy with a molar excess of from about 10:1 to about 300:1 of a nitrating agent in a suitable solvent in the presence of an amount of sulfuric acid that is less than equimolar relative to the amount of nitrating agent under conditions such that at least one pripheral aryl moiety is nitrated; and reducing the nitrated tetraarylporphyrin to its amino derivative.

Claim 35

A process for preparing an amino tetraarylporphyrin which comprises contacting a tetraarylporphyrin compound of the formula ##STR10## wherein each R independently represents hydrogen, aryl, alkyl, halo, alkylaryl, alkoxy, or carboalkoxy with a molar excess of from about 10:1 to about 300:1 of nitric acid in a suitable solvent in the presence of an amount of sulfuric acid that is less than equimolar relative to the amount of nitric acid under conditions such that at least one peripheral aryl moiety is nitrated at the para position; and reducing the nitrated tetraarylporphorin to its amino derivative.

Claim 36

A process for preparing an amino tetraarylporphyrin which comprises contacting a tetraarylporphyrin compound of the formula ##STR10## wherein each R independently represents hydrogen, aryl, alkyl, halo, alkylaryl, alkoxy, or carboalkoxy with a molar excess of from about 10:1 to about 300:1 of nitric acid in a suitable solvent in the presence of an amount of sulfuric acid that is less than equimolar relative to the amount of nitric acid under conditions such that at least one peripheral aryl moiety is nitrated at the para position; and reducing the nitrated tetraarylporphorin to its amino derivative.