# US 4,399,071 A · Method for making diaryliodonium salts

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- Number: US 4,399,071 A
- Document ID: US4399071A
- Status: Granted
- Kind: A
- Application number: 06/357,433
- Filed: 1982-03-12
- Granted: 1983-08-16
- Earliest claimed: 1982-03-12
- Assignees: General Electric Company
- Inventors: James V. Crivello; Julia L. Lee
- Web page: https://patentgrep.com/patent/US4399071A

## CPC

- C07C 49/675: having three rings
- C07C 17/093: by replacement by halogens
- C07C 25/18: Polycyclic aromatic halogenated hydrocarbons
- C07C 41/22: by introduction of halogens; by substitution of halogen atoms by other halogen atoms
- C07D 307/91: Dibenzofurans; Hydrogenated dibenzofurans
- C07C: ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07D: HETEROCYCLIC COMPOUNDS (macromolecular compounds C08)

## Abstract

A method is provided for making certain diaryliodonium salts which are useful as photoinitiators for a variety of cationic polymerizable organic materials. Reaction is effected between an aromatic iodo compound and an arylorganic aromatic compound in the presence of a peroxy organic acid and an organic sulfonic acid.

## Claims

### Claim 1

A method for making a diaryliodonium salt which comprises,
(1) incrementally adding a peracid to a C.sub.(1-13) iodo aryl compound to provide a mixture of from about 1-3 moles of peracid per mole of iodo aryl compound,
(2) combining the mixture of (1) with a mixture of a C.sub.(1-13) organic sulfonic acid and a C.sub.(6-13) aryl organic compound selected from a substituted and unsubstituted aromatic hydrocarbon to produce a mixture having about 1 mole of the C.sub.(1-13) organic sulfonic acid and about 1 mole of the aryl organic compound per mole of the iodo aryl compound,
(3) allowing the ingredients of (2) to react to produce a diaryliodonium organosulfonic acid salt,
(4) recovering the diaryliodonium organic sulfonic acid salt from (3),
(5) effecting a metathesis between the diaryliodonium organic acid salt of (4) and a polyfluoro metal or metalloid salt of the formula,
XMF.sub.d,
(6) recovering the resulting diaryliodonium polyfluoro metalloid salt from the mixture of (5), and
(7) washing the recovered diaryliodonium polyfluoro metalloid salt of (6) to effect removal therefrom of the by-product organic sulfonic acid metal salt,
where M is a metal or metalloid, X is an ion of an element selected from hydrogen, alkali metals and alkaline earth metals, and d is an integer equal to 4-6 inclusive.

### Claim 2

A method for making 4-methoxydiphenyliodonium hexafluoroantimonate which comprises
(1) incrementally adding peracetic acid to iodobenzene at a temperature of below about 40.degree. C. to provide a mixture having from about 1 to 3 moles of peracetic acid per mole of iodobenzene,
(2) combining the mixture of (1) with p-toluene sulfonic acid monohydrate and anisole to produce a mixture having about 1 mole of the p-toluene sulfonic acid monohydrate and anisole, per mole of the iodobenzene,
(3) allowing the ingredients of the mixture of (2) to react to produce 4-methoxyphenyliodonium tosylate,
(4) recovering the 4-methoxyphenyliodonium tosylate of (3),
(5) effecting methathesis between the 4-methoxyphenyliodonium tosylate and sodium hexafluoroantimonate,
(6) recovering the 4-methoxydiphenyliodonium hexafluoroantimonate from the mixture of (5) and
(7) washing the 4-methoxydiphenyliodonium hexafluoroantimonate to effect the removal therefrom of sodium p-toluene sulfonic acid monohydrate.

### Claim 3 (depends on 1)

A method in accordance with claim 1, where the iodo aryl compound is iodobenzene.

### Claim 4 (depends on 1)

A method in accordance with claim 1, where the aryl organic compound of (2) is allyl phenyl ether.

### Claim 5 (depends on 1)

A method in accordance with claim 1, where the aryl organic compound of (2) is biphenyl.

### Claim 6 (depends on 1)

A method in accordance with claim 1, where the aryl organic compound of (2) is phenylether.

### Claim 7 (depends on 1)

A method in accordance with claim 1, where the iodo aryl compound is iodoaryl toluene.

### Claim 8 (depends on 1)

A method in accordance with claim 1, where the aryl organic compound is dibenzofuran.