Biscarbodiimides and polycarbodiimides and method for their preparation

Patent metadata

Field	Value
Publication number	US-11104641-B2
Application number	US-201716078643-A
Country	US
Kind code	B2
Filing date	Mar 8, 2017
Priority date	Mar 31, 2016
Publication date	Aug 31, 2021
Grant date	Aug 31, 2021

Abstract

The present disclosure describes a method of synthesizing carbodiimides comprising providing an alkylisothiourea, providing a thiophilic reagent to the reaction mixture and reacting under conditions sufficient to provide the carbodiimide, and wherein the carbodiimide is a polycarbodiimide or a biscarbodiimide. The present disclosure further describes methods for isolating the carbodiimides. The present disclosure additionally describes isolated carbodiimide compositions.

First claim

What is claimed is:

1. A method of synthesizing polycarbodiimides or biscarbodiimides comprising:
(a) providing an alkylisothiourea of formula (1) to a reaction mixture;

where:
R 1 ═H; (C 1 -C 40 )hydrocarbyl;
R 2 ═(C 1 -C 40 )hydrocarbyl;
R 3 ═H; (C 1 -C 40 )hydrocarbyl;
R 4 ═H; or absent;
R 5 ═H; or absent;
R 6 ═(C 1 -C 40 )alkyl;
R 7 ═H; (C 1 -C 40 )hydrocarbyl;
a is 0 or 1;
b is from 1 to 10; and
c is from 1 to 10;

(b) providing a thiophilic reagent to the reaction mixture and reacting under conditions sufficient to provide the polycarbodiimide or the biscarbodiimide, wherein the thiophilic reagent comprises halide, amine, nitrile, triflate, nitrate, acetate, acetylacetonate, carbonate, oxalate, oxide, phosphate, sulfite, sulfate of copper, zinc, gold, molybdenum, mercury, tungsten, nickel, silver, iron, cobalt, or manganese.

2. The method of synthesizing carbodiimides of claim 1 , wherein the reaction mixture further comprises a solvent selected from the list consisting of acetonitrile, proprionitrile, butyronirile, isobutyronitrile, valeronitrile, hexanenitrile, trimethylacetonitrile, malonitrile, succionitrile, glutaronitrile, adiponitrile, 1,5-dicyanopentane, 1,6-dicyanohexane, N,N-dimethylformamide, N,N-dimethyl acetamide, acetone, methylene chloride, 1,2-dichloroethane, chloroform, carbontetrachloride, 1,4-dioxane, benzene, toluene, xylenes, pentane, hexanes, heptanes, petroleum ether, diethyl ether, tetrahydrofuran, 2-methyltetrahydrofuran, methyl-t-butyl ether, or a mixture thereof.

3. The method of synthesizing carbodiimides of claim 1 , wherein the reaction mixture further comprises a base selected from the list consisting of acyclic or cyclic N,N,N-trisubstituted amine.

4. The method of synthesizing carbodiimides of claim 1 , wherein the reaction mixture has an operating temperature of from −78 to 50° C.

5. The method of synthesizing carbodiimides of claim 1 , wherein the thiophilic reagent comprises a metal that is not an alkali metal.

6. The method of synthesizing carbodiimides of claim 1 , wherein the thiophilic reagent comprises a metal that is a transition metal.

7. The method of synthesizing carbodiimides of claim 1 , wherein the thiophilic reagent is selected from the group consisting of a halide, amine, nitrile, triflate, nitrate, acetate, acetylacetonate, carbonate, oxalate, oxide, phosphate, sulfite, or sulfate of silver.

8. The method of synthesizing carbodiimides of claim 1 , wherein the thiophilic reagent is silver nitrate.

Assignees

• Dow Global Technologies Llc

Inventors

• Camelio Andrew M
• Krasovskiy Arkady L

Classifications

• C07C2601/16

  the ring being unsaturated · CPC title

• C07C2603/74

  Adamantanes · CPC title

• B01J2523/24

  Strontium · CPC title

• B01J2523/13

  Potassium · CPC title

• B01J27/236

  Hydroxy carbonates · CPC title