Manganese based complexes and uses thereof for homogeneous catalysis

Patent metadata

Field	Value
Publication number	US-12145139-B2
Application number	US-202318351557-A
Country	US
Kind code	B2
Filing date	Jul 13, 2023
Priority date	Feb 9, 2016
Publication date	Nov 19, 2024
Grant date	Nov 19, 2024

Abstract

The present invention relates to novel manganese complexes and their use, inter alia, for homogeneous catalysis in (1) the preparation of imine by dehydrogenative coupling of an alcohol and amine; (2) C—C coupling in Michael addition reaction using nitriles as Michael donors; (3) dehydrogenative coupling of alcohols to give esters and hydrogen gas (4) hydrogenation of esters to form alcohols (including hydrogenation of cyclic esters (lactones) or cyclic di-esters (di-lactones), or polyesters); (5) hydrogenation of amides (including cyclic dipeptides, lactams, diamide, polypeptides and polyamides) to alcohols and amines (or diamine); (6) hydrogenation of organic carbonates (including polycarbonates) to alcohols or hydrogenation of carbamates (including polycarbamates) or urea derivatives to alcohols and amines; (7) dehydrogenation of secondary alcohols to ketones; (8) amidation of esters (i.e., synthesis of amides from esters and amines); (9) acylation of alcohols using esters; (10) coupling of alcohols with water and a base to form carboxylic acids; and (11) preparation of amino acids or their salts by coupling of amino alcohols with water and a base. (12) preparation of amides (including formamides, cyclic dipeptides, diamide, lactams, polypeptides and polyamides) by dehydrogenative coupling of alcohols and amines; (13) preparation of imides from diols.

First claim

What is claimed is:

1. A manganese complex represented by the structure of any of formula VI, VIA, VIB, VIC or their isomer or salt thereof:

wherein
L 1 is (PR a R b ), (NR a R b ), imine; oxazoline, sulfide (SR a ), sulfoxide (S(═O) R a ), heteroaryl containing at least one heteroatom selected from nitrogen and sulfur; (AsR a R b ), (SbR a R b ) or a N-heterocyclic carbene represented by the structures:

L 2 is (PR a R b ), (NR a R b ), imine; oxazoline, sulfide (SR a ), sulfoxide (S(═O) R a ), heteroaryl containing at least one heteroatom selected from nitrogen and sulfur; (AsR a R b ), (SbR a R b ) or a N-heterocyclic carbene represented by the structures:

L 3 and L 4 are each independently a mono-dentate two-electron donor selected from the group consisting of CO, PR a R b R c , P(OR a )(OR b )(OR c ), NO + , AsR a R b R c , SbR a R b R c , NR a R b R c , SR a R b , nitrile (RCN), isonitrile (RNC), N 2 , PF 3 , CS, heteroaryl, tetrahydrothiophene, alkene, alkyne or L 3 and L 4 form together with the Mn a ring;
L 5 is absent or a mono-dentate two-electron donor selected from the group consisting of, CO, PR a R b R c , P(OR a )(OR b )(OR c ), NO + , NR a R b R c , AsR a R b R c , SbR a R b R c , SR a R b , nitrile (RCN), isonitrile (RNC), N 2 , PF 3 , CS, heteroaryl, tetrahydrothiophene, alkene or alkyne;
X is halide, OCOR, OCH 2 Q, OCOCF 3 , OSO 2 R, OSO 2 CF 3 , CN, OR, N(R) 2 and RS, BF 4 , B(C 6 H 5 ) 4 , B(C 6 F 5 ) 4 , B[(C 6 H 4 )(CF 3 ) 2 ], PF 6 or ClO 4 ;
X′ is H, halide, OCOR, OCH 2 Q, OCOCF 3 , OSO 2 R, OSO 2 CF 3 , CN, OR, N(R) 2 or RS;
Q is hydrogen, alkyl, cycloalkyl, aryl, heterocyclyl, heteroaryl, alkylcycloalkyl, alkylaryl, alkylheterocyclyl or alkylheteroaryl;
Y + is a cationic group bearing a single positive charge;
R, R a R b and R c are each independently H, alkyl, cycloalkyl, aryl, heterocyclyl, heteroaryl, alkylcycloalkyl, alkylaryl, alkylheterocyclyl or alkylheteroaryl;
R j , R k and R l are each independently H, alkyl, cycloalkyl, aryl, heterocyclyl, heteroaryl, alkylcycloalkyl, alkylaryl, alkylheterocyclyl or alkylheteroaryl; and
Z is zero, one, two or three substituents wherein each such substituent is independently selected from the group consisting of alkyl, cycloalkyl, aryl, heterocyclyl, heteroaryl, alkylcycloalkyl, alkylaryl, alkylheterocyclyl, alkylheteroaryl, halogen, nitro, amide, ester, cyano, alkoxy, alkylamino, arylamino, an inorganic support and a polymeric moiety.

2. The complex of claim 1 , wherein X′ is bromide.

3. The complex of claim 1 , wherein X′ is hydride.

4. The complex of claim 1 , wherein L 1 is phosphine (PR a R b ).

5. The complex of claim 1 , wherein L 2 is phosphine (PR a R b ).

6. The complex of claim 1 , wherein L 1 is amine (NR a R b ).

7. The complex of claim 1 , wherein L 3 and L 4 are CO.

8. The complex of claim 1 , wherein Z is zero substituents and said aryl group is unsubstituted.

9. The complex of claim 1 , wherein said complex is represented by the structure of formula VI(1):

10. The complex of claim 1 wherein L 1 and L 2 is phosphine (PR a R b ), wherein R a and R b are each independently selected from the group consisting of H, methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, t-butyl and benzyl.

11. The complex of claim 10 , wherein R a and R b are isopropyl.

12. The complex of claim 11 wherein said complex is represented by the structure of formula 18:

13. The complex of claim 1 , wherein said complex is represented by the structure of formula VIB(1):

14. The complex of claim 13 , wherein said complex is represented by the structure of formula 19:

15. The complex of claim 13 , wherein said complex is represented by the structure of formula 20:

16. The complex of claim 1 , wherein said complex is represented by the structure of formula VIC(1):

17. The complex of claim 16 , wherein said complex is represented by the structure of formula 21:

18. A catalytic process for preparing an formamide by dehydrogenative coupling of methanol and amine of formula R 27 R 27′ NH:

wherein
R 27 and R 27′ are each independently selected from the group consisting of H, an unsubstituted or substituted, saturated or unsaturated: alkyl, alkoxyalkyl, cycloalkyl, aryl, alkylaryl, heterocyclyl and heteroaryl;
wherein said process comprising the step of reacting said methanol and said amine in the presence of the manganese complex according to claim 1 , thereby generating an amide; wherein if a manganese complex of formula VIA, is used as a catalyst, an amount of base equivalent to the amount of catalyst or higher is added.

19. The process of claim 18 herein said complex is a complex of formula 18, 19, 20 or 21:

Assignees

• Yeda Res & Dev
• Nerush Arkadi

Inventors

• Milstein David
• Nerush Alex
• Vogt Matthias
• Mukherjee Arup
• Espinosa-Jalapa Noel Angel
• Chakraborty Subrata

Classifications

• C07C249/02

  of compounds containing imino groups · CPC title

• C07B43/08

  of cyano groups · CPC title

• C07B43/06

  of amide groups · CPC title

• B01J2531/72

  Manganese · CPC title

• B01J2231/348

  1,4-additions, e.g. conjugate additions · CPC title