The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Patent No.:

US 7026478 B1

PDF
Full Text
Expired
Date of Patent:
Apr. 11, 2006

Filed:

May. 10, 2002
Applicants:

Alois Fürstner, Mülheim an der Ruhr, DE;

Andreas Leitner, Mülheim an der Ruhr, DE;

María Méndez, Mülheim an der Ruhr, DE;

Inventors:

Alois Fürstner, Mülheim an der Ruhr, DE;

Andreas Leitner, Mülheim an der Ruhr, DE;

María Méndez, Mülheim an der Ruhr, DE;

Assignee:

Studiengesellschaft Kohle mbH, Mulheim an der Ruhr, DE;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C07D 237/00 (2006.01); C07D 237/02 (2006.01); C07D 487/00 (2006.01); C07D 251/00 (2006.01); C07D 239/02 (2006.01); C07D 215/00 (2006.01); C07D 215/04 (2006.01); C07D 215/12 (2006.01); C07C 69/76 (2006.01); C07C 303/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

A process for the production of compounds Ar—Rby means of a cross-coupling reaction of an organometallic reagent R-M with an aromatic or heteroaromatic substrate Ar—X catalyzed by one or several iron salts or iron complexes as catalysts or pre-catalysts, present homogeneously or heterogeneously in the reaction mixture. This new invention exhibits substantial advantages over established cross coupling methodology using palladium- or nickel complexes as the catalysts. Most notable aspects are the fact that (i) expensive and/or toxic nobel metal catalysts are replaced by cheap, stable, commercially available and toxicologically benign iron salts or iron complexes as the catalysts or pre-catalysts, (ii) commercially attractive aryl chlorides as well as various aryl sulfonates can be used as starting materials, (iii) the reaction can be performed under 'ligand-free' conditons, and (iv) the reaction times are usually very short.


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