Substituted crown polyethers

Claim 2

A substituted crown polyether of the formula ##STR13## wherein (1) R 1 is a polymeric radical selected from reactive halogen containing polymers, homopolymers of acrylates, and copolymers containing acrylate functionality; (2) A is an alkylene group represented by the formula ##STR14## wherein p is zero or 1, R 2 to R 7 are each occurrence independently hydrogen or radicals having up to 15 carbons taken from a group consisting of alkyl, aryl and arylalkyl; (3) n is 3, 4, 5 or 6; and (4) q is an integer greater than or equal to one.

Claim 3

A substituted crown polyether according to claim 1 formed by covalently bonding a hydroxymethyl crown ether reactant of the formula ##STR15## wherein A is an alkylene group represented by the formula ##STR16## wherein p is zero or 1, R 2 to R 7 are each occurrence independently hydrogen or radicals having up to 15 carbons taken from a group consisting of alkyl, aryl, and arylalkyl, and n is 3, 4, 5 or 6, to a polymeric resin selected from a group consisting of cross-linked chloromethylated polystyrene, homopolymers of acrylates and copolymers of acrylates.

Claim 4

The substituted crown polyether according to claim 2 wherein A of the hydroxymethyl crown ether reactant is --CH 2 --CH 2 --.

Claim 5

The substituted crown polyether according to claim 2 wherein the hydroxymethyl crown ether reactant is covalently bonded to cross-linked, chloromethylated polystyrene beads.

Claim 6

The substituted crown polyether according to claim 4 wherein the cross-linked, chloromethylated polystyrene beads may vary in size from about American Standard mesh size 400 to about American Standard mesh size 16, being cross-linked from about 1 percent to about 10 percent and containing at least 0.1 meq of chlorine per gram of beads.

Claim 7

The substituted crown polyether according to claim 4 wherein the hydroxymethyl crown ether reactant is hydroxymethyl 18-crown-6 polyether.

Claim 8

In a nucleophilic substitution reaction process whereby a phase-transfer catalyst is utilized, the improvement wherein the phase-transfer catalyst is a substituted crown polyether of claim 1.

Claim 9

The process according to claim 7 wherein p is zero, and R 2 to R 7 are hydrogen.

Claim 10

The process according to claim 8 wherein the substituted crown ether phase-transfer catalyst is formed by covalently bonding hydroxymethyl 18-crown-6 polyether to a polymeric resin selected from a group consisting of cross-linked, chloromethylated polystyrene, homopolymers of acrylates, and copolymers of acrylates.

Claim 11

The process according to claim 9 wherein the polymeric resin is cross-linked, chloromethylated polystyrene beads.

Claim 12

The process according to claim 10 wherein the cross-linked, chloromethylated polystyrene beads may vary in size from about American Standard mesh size 400 to about American Standard mesh size 16, being cross-linked from about 1 percent to about 10 percent and containing at least 0.1 meq of chlorine per gram of beads.

Claim 13

The improved nucleophilic substitution process according to claim 10 wherein the reaction process is conducted at temperatures up to about 150° C.

Claim 14

A process for covalently bonding hydroxymethyl substituted crown ether compounds to cross-linked chloromethylated polystyrene beads comprising mixing hydroxymethyl substituted crown ether compounds of the formula ##STR17## wherein A is an alkylene group represented by the formula ##STR18## wherein p is zero or 1, R 2 to R 7 are each occurrence independently hydrogen or radicals having up to 15 carbons taken from a group consisting of alkyl, aryl, and arylalkyl; and n is 3, 4, 5 or 6, with an alkali metal hydride in an inert organic solvent selected from a group consisting of dimethyl formamide, dimethyl sulfoxide, alkylated polyethers, and a mixture of toluene and dioxane; adding cross-linked chloromethylated polystyrene; refluxing the mixture at an elevated temperature; and recovering the resulting product.

Claim 15

A process for covalently bonding hydroxymethyl substituted crown ether compounds to cross-linked chloromethylated polystyrene beads comprising mixing hydroxymethyl substituted crown ether compounds of the formula ##STR17## wherein A is an alkylene group represented by the formula ##STR18## wherein p is zero or 1, R 2 to R 7 are each occurrence independently hydrogen or radicals having up to 15 carbons taken from a group consisting of alkyl, aryl, and arylalkyl; and n is 3, 4, 5 or 6, with an alkali metal hydride in an inert organic solvent selected from a group consisting of dimethyl formamide, dimethyl sulfoxide, alkylated polyethers, and a mixture of toluene and dioxane; adding cross-linked chloromethylated polystyrene; refluxing the mixture at an elevated temperature; and recovering the resulting product.