Syntheses of N-heterocyclic carbenes and intermediates therefor

Patent metadata

Field	Value
Publication number	US-10759763-B2
Application number	US-201715852367-A
Country	US
Kind code	B2
Filing date	Dec 22, 2017
Priority date	Jan 8, 2013
Publication date	Sep 1, 2020
Grant date	Sep 1, 2020

Abstract

A method of preparing a 2,6 disubstituted anilines includes, reacting a 2-amino isophthalic acid diester with sufficient Grignard reagent R2CH2MgX to form the corresponding diol product, dehydrating the diol product to the corresponding dialkene; and hydrogenating the diol product to form the corresponding aniline. The 2,6 disubstituted anilines can be used to produce N-Heterocyclic Carbenes (NHCs). The NHCs can find application in various fields such as organic synthesis, catalysis and macromolecular chemistry. Palladium catalysts containing the NHCs are also described.

First claim

The invention claimed is:

1. An imidazolium salt of structure III;

wherein X − is a halogen anion, each R 2 is the same and is n-propyl; and wherein the groups Z 1 and Z 3 are H and the group Z 2 is selected from methyl, methoxy and —NMe 2 .

2. The imidazolium salt of claim 1 , wherein the groups Z 1 and Z 3 are H and the group Z 2 is methyl or methoxy.

3. A metal complex comprising an N-heterocyclic carbene prepared from an imidazolium salt of structure XX;

wherein X − is a halogen anion, each R 2 is the same and selected from ethyl and n-propyl; and Z 1 , Z 2 , and Z 3 is a substituent independently selected from the group consisting of —H, —I, —CF 3 , —OR 5 , —R 6 and —NR 7 2 ; wherein each group R 5 ,R 6 or R 7 is independently selected from the group consisting of: alkyl that may be unsaturated, substituted alkyl that may be unsaturated, aryl, substituted aryl, aralkyl and substituted aralkyl;
or from an imidazolium salt of structure XVII or XXa:

wherein X − is an anion, the groups R 2 are the same and selected from H, methyl, ethyl, n-propyl and

wherein either R 3 is H and R 4 is alkyl that may be substituted, or
each of R 3 , R 4 are an independently selected alkyl that may be substituted; and
Z 1 , Z 2 , Z 3 are independently selected from the group consisting of: —H, —I, —CF 3 , —OR 5 , —R 6 and —NR 7 2 ;
wherein each group R 5 , R 6 or R 7 is independently selected from the group consisting of: alkyl that may be unsaturated, substituted alkyl that may be unsaturated, aryl, substituted aryl, aralkyl and substituted aralkyl.

4. A method of preparing an N-heterocyclic carbene, the method comprising:
reacting an aniline of general formula I:

wherein each group R 2 is n-propyl; and
wherein the groups Z 1 , Z 2 and Z 3 are H;

with glyoxal to form a diimine of general formula II;

cyclizing the diimine of structure II with paraformaldehyde to form an imidazolium salt of structure Ill;

wherein X − is an anion; and

reacting the imidazolium salt of structure Ill with a base to form the N-heterocyclic carbene.

Assignees

• Umicore Ag & Co Kg

Inventors

• Nolan Steven P
• Meiries Sebastien

Classifications

• B01J2531/824

  Palladium · CPC title

• C07C211/47

  Toluidines; Homologues thereof · CPC title

• C07D295/037

  with quaternary ring nitrogen atoms · CPC title

• C07C227/04

  Formation of amino groups in compounds containing carboxyl groups · CPC title

• C07C211/45

  Monoamines · CPC title