IP Library Granted Patent US 6,921,731
Granted Patent B2
US 6,921,731 · App. 10/297,237 · Granted Jul 26, 2005

Process for regenerating Pd catalysts

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,921,731
App. No.
10/297,237
Granted
Jul 26, 2005
Kind
B2
Abstract

Process for regenerating a Pd catalyst after a homogeneously catalyzed C—C coupling reaction in which the Pd catalyst precipitates, is separated from the reaction mixture and subsequently treated with I 2 or Br 2 . The Pd catalyst can then be used in a subsequent reaction run. Preferably between 1 and 3 mole equivalents of I 2 or Br 2 , relative to the quantity of Pd catalyst is used The C—C coupling reaction is preferably carried out in the presence of a support material. The C—C coupling reaction may be for example a Heck reaction, a Suzuki reaction or a cross-coupling reaction.

Claims (15)

1. A method for a homogeneously catalyzed C—C coupling, comprising conducting a C—C coupling using a Pd catalyst that is regenerated by treating a precipitated Pd catalyst, after separation from a reaction mixture, with iodine or bromine.

2. The method of claim 1 , wherein the regenerated Pd catalyst is added to an additional reaction mixture for a C 13 C coupling reaction.

3. The method of claim 2 , wherein the ratio of equivalents of bromine or iodine to equivalents of precipitated and separated Pd catalyst is between 1 and 3.

4. The method of claim 2 , wherein said Pd catalyst is Pd(OAc) 2 , PdCl 2 , PdBr 2 , PdCl 2 , Na 2 PdCl 4 , Na 2 PdCl 6 , Pd 2 (dba) 3 (dba =dibenzyliden acetone), PdCl 2 (PhCN) 2 , PdCl 2 (CH 3 CN) 2 , Pd clusters or Pd metal.

5. The method of claim 1 , wherein said treating step is performed in situ in an additional reaction mixture for conducting a C—C coupling reaction.

6. The method of claim 5 , wherein the ratio of equivalents of bromine or iodine to equivalents of precipitated and separated Pd catalyst is between 1 and 3.

7. The method of claim 5 , wherein said Pd catalyst is Pd(OAc) 2 , PdCl 2 , PdBr 2 , PdCl 2 , Na 2 PdCl 4 , Na 2 PdCl 6 , Pd 2 (dba) 3 (dba=dibenzyliden acetone), PdCl 2 (PhCN) 2 , PdCl 2 (CH 3 CN) 2 , Pd clusters or Pd metal.

8. The method of claim 1 , wherein the ratio of equivalents of bromine or iodine to equivalents of precipitated and separated Pd catalyst is between 1 and 3.

9. The method of claim 1 , wherein said Pd catalyst is Pd(OAc) 2 , PdCl 2 , PdBr 2 , PdCl 2 , Na 2 PdCl 4 , Na 2 PdCl 6 , Pd 2 (dba) 3 (dba=dibenzylidene acetone), PdCl 2 (PhCN) 2 , PdCl 2 (CH 3 CN) 2 , Pd clusters or Pd metal.

10. The method of claim 1 , wherein the reaction mixture further contains a support material.

11. The method of claim 1 , wherein the C—C coupling reaction is a Heck reaction.

12. The method of claim 1 , wherein the C—C coupling reaction is a Suzuki reaction.

13. The method of claim 1 , wherein the C—C coupling reaction is a cross-coupling reaction.

14. The method of claim 1 , comprising conducting an additional C—C coupling using a precipitated Pd catalyst that is regenerated after separation from a first C—C coupling reaction mixture.

15. The method of claim 1 , comprising conducting an additional C—C coupling using a precipitated Pd catalyst from a first C—C coupling reaction mixture, wherein iodine or bromine is added as a first reagent in said additional C—C coupling reaction.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 5, 2004
From: DSM N.V.
To: DSM IP ASSETS B.V.
Reel/Frame 014863/0133 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 3, 2002
From: PARLEVLIET, FLORIS JACOBUS; VRIES DE, JOHANNES GERARDUS; VRIES DE, ANDREAS HENDRIKUS MARIA
To: DSM N.V.
Reel/Frame 014282/0576 →