Polycarbonate transesterification

Claim 2

A polycarbonate transesterification process comprising reacting mixtures of bis(ortho-haloaryl)carbonate/orthohaloaryl arylcarbonate and a dihydric phenol under transesterification reaction conditions.

Claim 3

The claim 1 process where the bis(ortho-haloaryl)carbonate is of the formula: ##STR7## where at least a P or Q substituent is an ortho-positioned halogen or a trifluoromethyl group directly bonded to a ring carbon atom located adjacent to an oxy group of the carbonate, i and j represent whole numbers of at least 1 up to a maximum equivalent to the number of replaceable hydrogen atoms or alkyl groups substituted for on the aromatic rings comprising Ar and Ar', and the ortho-haloaryl arylcarbonate is of the formula: ##STR8## where P, i, and Ar are as defined above, Ar' being an aromatic ring.

Claim 4

The claim 1 process where the dihydric phenol is of the formula: ##STR9## where independently each R is hydrogen, C 1-4 alkyl, methoxy, bromine or chlorine, R g and R h are hydrogen or a C 1-30 monovalent hydrocarbon or hydrocarbonoxy group or of the formula: ##STR10## where independently each R is as defined previously and each Z is hydrogen, chlorine or bromine, subject to the proviso that at least one 2 is chlorine or bromine.

Claim 5

The claim 2 process where the transesterification reaction conditions employ a metal hydride catalyst selected from the class consisting of alkali metal, alkaline earth metal, quaternary ammonium, quaternary phosphonium, tertiary sulfonium aluminum hydrides and boron hydrides.

Claim 6

The claim 4 process where the metal hydride catalyst is a pre-formed mixture of a metal hydride and a bis(ortho-haloaryl)carbonate, an ortho-haloaryl aryl carbonate or a dihydric phenol.

Claim 7

The claim 1 process where the transesterification reaction conditions are at temperatures less than about 300° C.

Claim 8

The claim 6 process where the transesterification reaction conditions include an inert atmosphere.

Claim 9

The claim 2 process where the carbonate mixture is bis(o-chlorophenyl) carbonate and o-chlorophenyl phenyl carbonate.

Claim 10

The claim 3 process where the dihydric phenol is bis(4-hydroxyphenyl)propane-2,2.

Claim 11

A polycarbonate transesterification process comprising reacting a mixture of bis(ortho-chlorophenyl)carbonate and o-chlorophenyl phenyl carbonate with bis-(4-hydroxyphenyl)propane-2,2 under transesterification conditions.

Claim 12

A polycarbonate transesterification process comprising reacting a mixture of bis(ortho-chlorophenyl)carbonate and o-chlorophenyl phenyl carbonate with bis-(4-hydroxyphenyl)propane-2,2 under transesterification conditions.