Method of Preparing Hyperbranched Polyether Ester

Patent metadata

Field	Value
Publication number	US-2018194893-A1
Application number	US-201715559427-A
Country	US
Kind code	A1
Filing date	Apr 17, 2017
Priority date	May 12, 2016
Publication date	Jul 12, 2018
Grant date	—

Abstract

The present invention relates to a method of preparing a hyperbranched polyether ester. According to the present invention, a di-functionality haloalkane and a tri-functionality hydroxyl/carboxyl benzene are used as raw materials, and the hyperbranched polyether ester is synthetized in one pot with an A 2 +B 3 polymerization method. The present invention is featured by easily obtained raw materials and simple steps, and the prepared hyperbranched polyether ester contains end groups with high reactive activity, so that various functional groups or polymer chains can be introduced into the hyperbranched polyether ester by a further condensation reaction, ring-opening reaction, etc., and thus a hyperbranched polymer with a diversity of properties and unique functions can be prepared.

First claim

What is claimed is:

1 . A method of preparing a hyperbranched polyether ester, comprising the following steps:
using di-functionality haloalkane and tri-functionality hydroxyl/carboxyl benzene as raw materials, and synthetizing hyperbranched polyether ester with/without a central core molecule in one pot and with an A 2 +B 3 polymerization method; wherein the hyperbranched polymer ester is terminated by reactive groups including phenolic hydroxyl group, carboxyl group or haloalkyl, wherein the hyperbranched polymer ester has a number-average molecular weight of 5˜20 KDa, a polydispersity index of 1.3˜2, and a degree of branching of 0.5˜0.8; wherein a structure of the hyperbranched polyether ester is as follows:

2 . The method of preparing a hyperbranched polyether ester according to claim 1 , wherein the hyperbranched polyether ester is synthetized without a central core molecule in one pot, comprising steps as follows:
adding reactants comprising the tri-functionality hydroxyl/carboxyl benzene, the di-functionality haloalkane, an acid-binding agent, and a solvent into a reactor at one time, reacting under 20˜100° C. for 4˜96 h, adding an inorganic acid for acidification after the reaction to obtain a solution, filtering out a precipitate of the solution to obtain a filtrate, precipitating and purifying the filtrate in a precipitant, and drying to obtain a viscous solid colorless or in faint yellow; wherein an amount of the tri-functionality hydroxyl/carboxyl benzene is 1 mol, an amount of the di-functionality haloalkane is 0.75-3 mol, an amount of the acid-binding agent is 1.5-7.2 mol, and an amount of the solvent is 0.1-1 mol.

3 . The method of preparing a hyperbranched polyether ester according to claim 2 , wherein the tri-functionality hydroxyl/carboxyl benzene is selected from the group consisting of: 3,5-dihydroxy benzoic acid, 2,4-dihydroxy benzoic acid, 3,4-dihydroxy benzoic acid, 2,6-dihydroxy benzoic acid, 2,3-dihydroxy benzoic acid and 5-hydroxyisophthalic acid.

4 . The method of preparing a hyperbranched polyether ester according to claim 2 , wherein the di-functionality haloalkane is selected from the group consisting of: 1,10-dibromodecane, 1,2-dibromoethane, 1,6-dibromohexane, 1,12-dibromododecane, 1,11-dibromoundecane, 1,9-dibromononane, 1,7-dibromoheptane, 1,8-dibromooctane, 1,5-dibromopentane, 1,4-dibromobutane, 1,3-dibromopropane, 1,10-dichlorodecane, 1,2-dichloroethane, 1,6-dichlorohexane, 1,12-dichlorododecane, 1,11-dichloroundecane, 1,9-dichlorononane, 1,7-dichloroheptane, 1,8-dichlorooctane, 1,5-dichloropentane, 1,4-dichlorobutane, and 1,3-dichloropropane.

5 . The method of preparing a hyperbranched polyether ester according to claim 2 , wherein the acid-binding agent is selected from the group consisting of: sodium carbonate, potassium carbonate and sodium hydroxide.

6 . The method of preparing a hyperbranched polyether ester according to claim 2 , wherein the solvent is selected from the group consisting of: 1,4-dioxane, tetrahydrofuran, N,N′-dimethylformamide, N,N′-dimethylacetamide and N-methyl-pyrrolidone.

7 . The method of preparing a hyperbranched polyether ester according to claim 2 , wherein the inorganic acid is selected from the group consisting of: hydrochloric acid, sulfuric acid and nitric acid.

8 . The method of preparing a hyperbranched polyether ester according to claim 2 , wherein the precipitant is selected from the group consisting of: deionized water, anhydrous diethyl ether, petroleum ether, ethanol and deionized water mixed in equal ratios, methanol and deionized water mixed in equal ratios, and diethyl ether and petroleum ether mixed in equal ratios.

9 . The method of preparing a hyperbranched polyether ester according to claim 1 , wherein the hyperbranched polyether ester is synthetized with a central core molecule in one pot, wherein the reactants further comprising a central “core molecule”, wherein an amount of the central “core molecule” is 0.012-0.024 mol

10 . The method of preparing a hyperbranched polyether ester according to claim 9 , wherein the central “core molecule” is selected from the group consisting of: 1,3,5-benzene tricarboxylic acid, phloroglucinol, 1,3,5-benzene trimethanol.

Assignees

• Univ Jiangnan

Inventors

• Li Xiaojie
• Liu Xingliang
• Luo Jing
• Liu Xiaoya
• Chen Mingqing

Classifications

• C08G63/78

  Preparation processes · CPC title

• C08G63/664 Primary

  derived from hydroxy carboxylic acids · CPC title

• C08G63/682

  containing halogens · CPC title

• C08G63/6822

  derived from hydroxy carboxylic acids · CPC title

• C08G63/81

  using solvents (C08G63/79 takes precedence) · CPC title