Novel 2-amido- or 2-amino-alkyl ethers of polyhydric polyphenols and process for preparing same

Claim 2

A process for preparing a compound of the formula ##STR11## wherein R is a chemical bond, oxygen, sulfur, alkylene or alkylidene; W is hydrogen or a (--CR 1 R 2 --CR 3 R 4 --NHR 5 ) group with the proviso that at least two W groups are (--CR 1 R 2 --CR 3 R 4 --NHR 5 ) groups; wherein R 1 -R 4 are each independently hydrogen, lower alkyl or hydroxy-substituted lower alkyl; R 5 is a ##STR12## group, wherein R 6 is hydrogen, hydrocarbyl or inertly substituted hydrocarbyl; X, Y and Z are each independently inert substituents; m and p are each independently integers of from zero to four, inclusive; n is an integer of from zero to three, inclusive; q is a number of from zero to about ten; and M is alkylene or alkylidene, comprising reacting by contacting a 2-oxazoline of the formula: ##STR13## with a polyhydric polyphenol of the formula: ##STR14## in the presence of a small but catalytic amount of at least tin or one transition metal salt, said transition metal salt catalyst being a salt of a metal in groups 1b, 2b, 6b, 7b and 8 which is included in rows 4 and 5 of the Periodic Table of the Elements, inclusive.

Claim 3

The process defined by claim 1 wherein said transition metal salt catalyst is zinc acetate.

Claim 4

The process defined by claim 1 wherein said reaction is carried out at a temperature of from about 125° C. to 215° C.

Claim 5

The process defined by claim 1 wherein the equivalent ratio of said 2-oxazoline to the hydroxyl equivalents of said polyhydric polyphenol is from about 1:1 to about 1.3:1.

Claim 6

The process defined by claim 1 wherein said reaction is carried out in an inert atmosphere.

Claim 7

A process for preparing a compound of the formula ##STR15## wherein R is a chemical bond, oxygen, sulfur, alkylene or alkylidene; W is hydrogen or a (--CR 1 R 2 --CR 3 R 4 --NHR 5 ) group with the proviso that at least two W groups are (--CR 1 R 2 --CR 3 R 4 --NHR 5 ) groups; wherein R 1 -R 4 are each independently hydrogen, lower alkyl or hydroxy-substituted lower alkyl; R 5 is hydrogen; X, Y and Z are each independently inert substituents; m and p are each independently integers of from zero to four, inclusive; n is an integer of from zero to three, inclusive; q is a number of from zero to about ten; and M is alkylene or alkylidene, which comprises: (a) reacting by contacting a 2-oxazoline of the formula: ##STR16## with a polyhydric polyphenol of the formula: ##STR17## wherein R 6 is hydrogen, hydrocarbyl or inertly-substituted hydrocarbyl, and the other substituents are defined above, in the presence of a catalytic amount of at least tin or one transition metal salt, said transition metal salt catalyst being a salt of a metal in groups 1b, 2b, 6b, 7b and 8 which is included in rows 4 and 5 of the Periodic Table of the Elements, inclusive; (b) reacting product from Step (a) with acid or base to effect hydrolysis, thereby forming a polyamine of the formula: ##STR18## as the free amine or acid salt thereof.

Claim 8

A process for preparing a compound of the formula ##STR15## wherein R is a chemical bond, oxygen, sulfur, alkylene or alkylidene; W is hydrogen or a (--CR 1 R 2 --CR 3 R 4 --NHR 5 ) group with the proviso that at least two W groups are (--CR 1 R 2 --CR 3 R 4 --NHR 5 ) groups; wherein R 1 -R 4 are each independently hydrogen, lower alkyl or hydroxy-substituted lower alkyl; R 5 is hydrogen; X, Y and Z are each independently inert substituents; m and p are each independently integers of from zero to four, inclusive; n is an integer of from zero to three, inclusive; q is a number of from zero to about ten; and M is alkylene or alkylidene, which comprises: (a) reacting by contacting a 2-oxazoline of the formula: ##STR16## with a polyhydric polyphenol of the formula: ##STR17## wherein R 6 is hydrogen, hydrocarbyl or inertly-substituted hydrocarbyl, and the other substituents are defined above, in the presence of a catalytic amount of at least tin or one transition metal salt, said transition metal salt catalyst being a salt of a metal in groups 1b, 2b, 6b, 7b and 8 which is included in rows 4 and 5 of the Periodic Table of the Elements, inclusive; (b) reacting product from Step (a) with acid or base to effect hydrolysis, thereby forming a polyamine of the formula: ##STR18## as the free amine or acid salt thereof.

Claim 9

The product resulting from the process defined by claim 6.

Claim 10

A thermally curable composition comprising an epoxy resin and a cross-linking amount of the polyamine defined by claim 6.

Claim 11

The process defined in claim 6, wherein R is isopropylidene.

Claim 12

The product resulting from the process defined in claim 9.

Claim 13

A thermally curable composition comprising an epoxy resin and a cross-linking amount of the polyamine defined by claim 9.

Claim 14

The process defined in claim 6, wherein the 2-oxazoline and polyhydric polyphenol in Step (a) are 2-ethyl-2-oxazoline and Bisphenol A, respectively.

Claim 15

The product resulting from the process defined in claim 12.