Diaromatic amine derivatives as antioxidants
View Patent ↗Diraromatic amine derivatives having the general formula: wherein n is from 0 to 5; m is from 0 to 4; each R substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group or two R substituents together with the carbon atom to which they are bonded are joined together to form an unsaturated, partially saturated or saturated C 3 -C 30 ring structure optionally containing one or more heteroatoms, each R 1 substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group and R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group optionally containing a functional group are provided. Also provided are lubricating oil compositions containing the diraromatic amine derivatives.
1. A diaromatic amine derivative having the general formula:
wherein n is from 0 to 5; m is from 0 to 4; each R substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group or two R substituents together with the carbon atom to which they are bonded are joined together to form an unsaturated, partially saturated or saturated C 3 -C 30 ring structure optionally containing one or more heteroatoms, each R 1 substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group and R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group optionally containing an ester group, an ether group, an aromatic group, or an amide group.
2. The diaromatic amine derivative of claim 1 , wherein R, R 1 , R 3 , R 4 , R 6 , and R 7 are hydrogen.
3. The diaromatic amine derivative of claim 1 , wherein R, R 1 , R 3 , R 4 , R 6 and R 7 are hydrogen and R 2 and R 5 independently are a C 1 -C 32 alkyl group optionally containing the ester group or the ether group.
4. The diaromatic amine derivative of claim 1 , wherein R, R 1 , R 3 , R 4 , R 6 and R 7 are hydrogen and R 2 and R 5 independently are a C 1 -C 12 alkyl group optionally containing the ester group or the ether group.
5. The diaromatic amine derivative of claim 1 , wherein two R groups together with the carbon atom to which they are bonded are joined together to form a saturated, unsaturated or partially saturated C 3 -C 30 ring structure optionally containing one or more heterocyclic groups.
6. A reaction mixture comprising two or more of the diaromatic amine derivatives of claim 1 .
7. A reaction mixture comprising two or more of the diaromatic amine derivatives of claim 2 .
8. A reaction mixture comprising two or more of the diaromatic amine derivatives of claim 3 .
9. A reaction mixture comprising two or more of the diaromatic amine derivatives of claim 4 .
10. A reaction mixture comprising two or more of the diaromatic amine derivatives of claim 5 .
11. A process for preparing one or more diaromatic amine derivatives having the general formula:
wherein n is from 0 to 5; m is from 0 to 4; each R substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group or two R substituents together with the carbon atom to which they are bonded are joined together to form an unsaturated, partially saturated or saturated C 3 -C 30 ring structure optionally containing one or more heteroatoms, each R 1 substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group and R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group optionally containing an ester group, an ether group, an aromatic group, or an amide group, the process comprising reacting a hydroxyl ethylene amine intermediate of the formula
wherein n, m, R, R 1 , R 2 , R 3 , R 4 , and R 5 have the aforementioned meanings, with a ketone or aldehyde.
12. A process for preparing one or more diaromatic amine derivatives having the general formula:
wherein n is from 0 to 5; m is from 0 to 4; each R substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group or two R substituents together with the carbon atom to which they are bonded are joined together to form an unsaturated, partially saturated or saturated C 3 -C 30 ring structure optionally containing one or more heteroatoms, each R 1 substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group and R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group optionally containing an ester group, an ether group, an aromatic group, or an amide group, the process comprising (a) reacting a substituted or unsubstituted N-phenyl-p-phenylenediamine derivative with an organic epoxide group; and (b) reacting the product of step (a) with a ketone or aldehyde.
13. The process of claim 12 , wherein the substituted or unsubstituted N-phenyl-p-phenylenediamine derivative is represented by the formula:
wherein n, m, R and R 1 have the aforementioned meanings.
14. The process of claim 12 ; wherein the substituted or unsubstituted N-phenyl-p-phenylenediamine derivative is selected from the group consisting of N-phenyl-p-phenylenediamine, N-phenyl-o-phenylenediamine, N-naphthyl-p-phenylenediamine, N-naphthyl-o-phenylenediamine, N-(5,6,7,8-tetrahydro-1-naphthyl)-p-phenylenediamine, N-(5,6,7,8-tetrahydro-2-naphthyl)-p-phenylenediamine, N-(5,6,7,8-tetrahydro-1-naphthyl)-o-phenylenediamine, N-(5,6,7,8-tetrahydro-2-naphthyl)-o-phenylenediamine, and combinations thereof.
15. The process of claim 12 , wherein the organic epoxide group is selected from the group consisting of an epoxidized hydrocarbon olefin, epoxidized vinyl ether, epoxidized vegetable oil, epoxidized unsaturated fatty esters of a vegetable oil and mixtures thereof.
16. The process of claim 12 , wherein the N-phenyl-p-phenylenediamine is N-p-phenylphenylenediamine and the organic epoxide group is selected from the group consisting of 1,2-epoxyalkyl, 1,2-epoxycycloalkyl and mixtures thereof.
17. The process of claim 12 , wherein the N-phenyl-p-phenylenediamine and organic epoxide group are reacted in a mole ratio of about 0.9:1 to about 1:1 of organic epoxide group to N-phenyl-p-phenylenediamine.
18. The process of claim 12 , wherein the ketone is selected from the group consisting of acetone, methyl ethyl ketone, diethyl ketone, methyl propyl ketone, methyl isopropyl ketone, ethyl propyl ketone, ethyl isopropyl ketone, dipropyl ketone, diisopropyl ketone, methyl butyl ketone, methyl isobutyl ketone, methyl sec butyl ketone, methyl tert-butyl ketone, ethyl butyl ketone, ethyl isobutyl ketone, ethyl sec-butyl ketone, ethyl tert-butyl ketone, propyl butyl ketone, isopropyl butyl ketone, propyl isobutyl ketone, propyl sec-butyl ketone, propyl tert butyl ketone, isopropyl isobutyl ketone, isopropyl sec-butyl ketone, isopropyl tert-butyl ketone, dibutyl ketone, diisobutyl ketone, di-sec-butyl ketone, di-tert-butyl ketone, butyl isobutyl ketone, butyl sec-butyl ketone, butyl tert-butyl ketone, isobutyl sec-butyl ketone, isobutyl tert-butyl ketone, sec-butyl tert-butyl ketone, 5-heptanone, 5-methyl-2-hexanone (methyl isoamyl ketone), 4-methyl-2-hexanone, 3-methyl-2-hexanone, 3,4-dimethyl-2-pentanone, 3,3-dimethyl-2-pentanone, 4,4-dimethyl-2-pentanone, 3-octanone, 4-methyl-3-heptanone, 5-methyl-3-heptanone, 6-methyl-3-heptanone, 4,4-dimethyl-3-hexanone, 4,5-dimethyl-3-hexanone, 5,5-dimethyl-3-hexanone, 4-nonanone, 5-methyl-4-octanone, 6-methyl-4-octanone, 7-methyl-4-octanone, 5,5-dimethyl-4-neptanone, 5,6-dimethyl-4-heptanone, 6,6-dimethyl-4-heptanone, 2-undecanone, cyclopropanone, cyclobutanone, cyclopentanone, cyclohexanone, cycloheptanone, cyclooctanone, cyclononanone, cyclodecanone, cycloundecanone, cyclododecanone and combinations thereof.
19. The process of claim 12 , wherein the aldehyde is selected from the group consisting of formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, 2-methylpropionaldehyde, valeraldehyde, 2-methyl-butanal, caproaldehyde, hexyldehyde, heptaldehyde, octaldehyde, nonaldehyde, decaldehyde, undecaldehyde, dodecaldehyde, benzaldehyde, phenylacetaldehyde, and combinations thereof.
20. The process of claim 12 , wherein the reaction of the substituted or unsubstituted N-phenyl-p-phenylenediamine derivative and the organic epoxide group is carried out in a suitable solvent and in the presence of an acid catalyst.
21. A lubricating oil composition comprising (a) at least one oil of lubricating viscosity and (b) an antioxidant improving effective amount of one or more diaromatic amine derivatives having the general formula:
wherein n is from 0 to 5; m is from 0 to 4; each R substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group or two R substituents together with the carbon atom to which they are bonded are joined together to form an unsaturated, partially saturated or saturated C 3 -C 30 ring structure optionally containing one or more heteroatoms, each R 1 substituent is independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group and R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are independently hydrogen or a straight or branched C 1 -C 32 alkyl group or alkenyl group optionally containing an ester group, an ether group, an aromatic group, or an amide group.
22. The lubricating oil composition of claim 21 , wherein R 1 , R 3 , R 4 , R 6 , R 7 and R are hydrogen.
23. The lubricating oil composition of claim 21 , wherein R 1 , R 3 , R 4 , R 6 , R 7 and R are hydrogen and R 2 and R 5 independently are a C 1 -C 32 alkyl group optionally containing the ester group or the ether group.
24. The lubricating oil composition of claim 21 , wherein R 1 , R 3 , R 4 , R 6 , R 7 and R are hydrogen and R 2 and R 5 independently are a C 1 -C 12 alkyl group optionally containing the ester group or the ether group.
25. The lubricating oil composition of claim 21 , wherein two R substituents together with the carbon atom to which they are bonded are joined together to form an unsaturated, partially saturated or saturated C 3 -C 30 ring structure optionally containing one or more heteroatoms.
26. The lubricating oil composition of claim 21 , wherein the at least one oil of lubricating viscosity is selected from the group consisting of engine oils, transmission fluids, hydraulic fluids, gear oils, marine cylinder oils, compressor oils, refrigeration lubricants and mixtures thereof.
27. The lubricating oil composition of claim 21 , wherein the at least one oil of lubricating viscosity has a viscosity of about 1.5 to about 2000 centistokes (cSt) at 100° C.
28. The lubricating oil composition of claim 21 , wherein the at least one oil of lubricating viscosity has a kinematic viscosity of about 1.5 cSt to about 30 cSt at 100° C.
29. The lubricating oil composition of claim 21 , wherein the at least one oil of lubricating viscosity has a kinematic viscosity of about 1.5 cSt to about 16 cSt at 100° C.
30. The lubricating oil composition of claim 21 , wherein the at least one oil of lubricating viscosity has a kinematic viscosity of about 1.5 cSt to about 12 cSt at 100° C.
31. The lubricating oil composition of claim 21 , wherein the at least one oil of lubricating viscosity has a SAE Viscosity Grade of 0W, 0W-20, 0W-30, 0W-40, 0W-50, 0W-60, 5W, 5W-20, 5W-30, 5W-40, 5W-50, 5W-60, 10W, 10W-20, 10W-30, 10W-40, 10W-50, 15W, 15W-20, 15W-30 or 15W-40.
32. The lubricating oil composition of claim 21 , further comprising at least one lubricating oil additive selected from the group consisting of antioxidants, anti-wear agents, detergents, rust inhibitors, dehazing agents, demulsifying agents, metal deactivating agents, friction modifiers, pour point depressants, antifoaming agents, co-solvents, package compatibilisers, corrosion-inhibitors, ashless dispersants, dyes, extreme pressure agents and mixtures thereof.
33. The lubricating oil composition of claim 21 , further comprising at least one lubricating oil additive selected from the group consisting of an alkylated diphenylamine, hindered phenolic, substituted or unsubstituted phenylenediamine, oil soluble copper compound, sulfur containing compound known to impart oxidation stability and mixtures thereof.
34. The lubricating oil composition of claim 33 , wherein the sulfur containing compound known to impart oxidation stability is selected from the group consisting of phenothiazines, sulfurized olefins, thiocarbamates, sulfur bearing hindered phenolic s, zinc dialkyldithiophosphates and mixtures thereof.
35. The lubricating oil composition of claim 21 , comprising a mixture of two or more of the diaromatic amine derivatives.
36. The lubricating oil composition of claim 21 , having a phosphorous content of less than about 0.1 weight percent.
37. The lubricating oil composition of claim 21 , having a phosphorous content of less than about 0.08 weight percent.
38. The lubricating oil composition of claim 21 , having a phosphorous content of less than about 0.05 weight percent.
39. An additive package comprising about 1 to about 75 weight percent of one or more of the diaromatic amine derivative of claim 1 .
40. An additive package comprising about 1 to about 75 weight percent of a reaction mixture comprising two or more of the diaromatic amine derivatives of claim 1 .
41. A stabilizer-containing composition comprising (a) an organic material subject to oxidative, thermal, and/or light-induced degradation and in need of stabilization to prevent or inhibit such degradation; and (b) a stabilization effective amount of one or more diaromatic amine derivatives of claim 1 .
42. The stabilizer-containing composition of claim 41 , wherein the organic material is selected from the group consisting of compounded tires, polyols, plastics, urethanes, greases, motor oils, rubber belts, cables, gaskets, seals and rubber products in the garment and carpet industries.
43. A method for stabilizing an organic material subject to oxidative, thermal, and/or light-induced degradation and in need of stabilization to prevent or inhibit such degradation, the method comprising adding to the organic material a stabilizing amount of one or more diaromatic amine derivatives of claim 1 .
44. The method of claim 43 , wherein the organic material is selected from the group consisting of compounded tires, polyols, plastics, urethanes, greases, motor oils, rubber belts, cables, gaskets, seals and rubber products in the garment and carpet industries.