Method of producing (meth)acryloyl-terminated polyisobutylene polymer

Patent metadata

Field	Value
Publication number	US-10604598-B2
Application number	US-201616061284-A
Country	US
Kind code	B2
Filing date	Dec 6, 2016
Priority date	Dec 11, 2015
Publication date	Mar 31, 2020
Grant date	Mar 31, 2020

Abstract

A method for producing a (meth)acryloyl-terminated polyisobutylene polymer includes a step 1 of polymerizing an isobutylene monomer under the presence of a Lewis acid catalyst to prepare a halogen-terminated polyisobutylene polymer (B), a step 2 of reacting the halogen-terminated polyisobutylene polymer (B) with a compound (C) having a halogen group and a phenoxy group under the presence a Lewis acid catalyst to prepare a halogenated phenoxyalkyl-terminated polyisobutylene polymer (D), and a step 3 of reacting the halogenated phenoxyalkyl-terminated polyisobutylene polymer (D) with an acrylic acid compound (E) to prepare the (meth)acryloyl-terminated polyisobutylene polymer (A).

First claim

The invention claimed is:

1. A method for producing a (meth)acryloyl-terminated polyisobutylene polymer (A) represented by the following general formula (1),

wherein R 1 represents a monovalent or multivalent aromatic hydrocarbon group, or a monovalent or multivalent aliphatic hydrocarbon group, A represents a polyisobutylene polymer, R 2 represents a divalent saturated hydrocarbon group having 2 to 6 carbons and having no heteroatom, each of R 3 and R 4 represents a hydrogen, a monovalent hydrocarbon having 1 to 20 carbons, or an alkoxy group, R 5 represents a hydrogen or a methyl group, and n represents natural number,
the method comprising:
a step 1 of polymerizing an isobutylene monomer under the presence of a Lewis acid catalyst to prepare a polyisobutylene polymer (B) represented by the following general formula (2),

wherein R 1 , A, and n are the same as in the general formula (1), and Z represents a chlorine, a bromine, an iodine, an acetoxy group, or a methoxy group;
a step 2 of reacting the polyisobutylene polymer (B) with a compound (C) having a halogen group and a phenoxy group as represented by the following general formula (3) under the presence of a Lewis acid catalyst to prepare a halogenated phenoxyalkyl-terminated polyisobutylene polymer (D) represented by the following general formula (4),
wherein a ratio of a total molar amount of the Lewis acid catalyst to a molar amount of the compound (C) having a halogen group and a phenoxy group is 3.3 or less,

wherein R 2 , R 3 , and R 4 are the same as in the general formula (1), and X represents a chlorine, a bromine, or an iodine,

wherein R 1 , R 2 , R 3 , R 4 , A, and n are the same as in the general formula (1), and X is the same as in the general formula (3); and
a step 3 of reacting the halogenated phenoxyalkyl-terminated polyisobutylene polymer (D) with an acrylic acid compound (E) represented by the following general formula (5) to prepare the (meth)acryloyl-terminated polyisobutylene polymer (A),

wherein R 5 represents a hydrogen or a methyl group, and Y represents a hydrogen, a lithium, a sodium, a potassium, a rubidium, or a cesium.

2. The method according to claim 1 , wherein a reaction solvent is used in the step 3, and wherein the reaction solvent is at least one solvent selected from the group consisting of a halogenated hydrocarbon, a linear saturated hydrocarbon, a cyclic saturated hydrocarbon, and an aromatic hydrocarbon.

3. The method according to claim 1 , wherein a reaction solvent is used in the step 3, and wherein the reaction solvent is a halogenated hydrocarbon, or a mixed solvent of a halogenated hydrocarbon and a linear saturated hydrocarbon.

4. The method according to claim 1 , wherein a reaction solvent is used in the step 3, and wherein the reaction solvent is an aromatic hydrocarbon, or a mixed solvent of an aromatic hydrocarbon and a linear saturated hydrocarbon or a cyclic saturated hydrocarbon.

5. The method according to claim 1 , wherein the step 3 is carried out under the presence of at least one compound selected from the group consisting of an ammonium salt, a phosphonium salt, and a crown ether.

6. The method according to claim 5 , wherein the ammonium salt comprises one or less of a methyl group as a substituent on a nitrogen atom.

7. The method according to claim 1 , further adding an aprotic amphiphilic solvent in the step 3.

8. The method according to claim 1 , wherein a content of water is 1000 ppm or less in the step 3.

9. The method according to claim 1 , wherein the (meth)acryloyl-terminated polyisobutylene polymer has a number average molecular weight of 8000 to 500000 as measured by size exclusion chromatography.

10. The method according to claim 1 , wherein in the chemical formula 5, Y represents a lithium, a sodium, a potassium, a rubidium, or a cesium.

Assignees

• Kaneka Corp

Inventors

• Ikari Yoshihiro

Classifications

• C08F10/10 Primary

  Isobutene · CPC title

• C08F2810/40

  taking place solely at one end or both ends of the polymer backbone, i.e. not in the side or lateral chains · CPC title

• C08F2810/30

  leading to the formation or introduction of aliphatic or alicyclic unsaturated groups · CPC title

• C08F110/10

  Isobutene · CPC title

• C08F8/18

  Introducing halogen atoms or halogen-containing groups · CPC title