Cyclic thioamides as additives for lubricating oils

Abstract

A composition comprising: (a) from 0.1% to 20% of at least one cyclic thioamide of formula I: 1

Description

BACKGROUND

[0001] This invention relates generally to cyclic thioamides useful as additives for lubricating oils.

[0002] Zinc dialkyldithiophosphates (ZDDP) are widely used as lubricant additives. The principal disadvantages of these compounds are that an ash residue is produced by the zinc as the additive is consumed, and that phosphorus is known to affect the efficiency of catalytic converters in motor vehicles, thereby causing emissions problems. Cyclic compounds useful as lubricant additives are disclosed in U.S. Pat. No. 6,187,722. However, the compounds disclosed therein are imidazolidinethiones which are not within the scope of the present invention.

[0003] The problem addressed by this invention is to find additional non-metallic, non-phosphorus-containing oil-soluble additives for lubricating oils.

STATEMENT OF INVENTION

[0004] The present invention is directed to a composition comprising:

[0005] (a) from 0.1% to 20% of at least one cyclic thioamide of formula I: 2

[0006]  wherein X is CR5R6, CR5R6NR7 or CR5R6CR8R9; R1, R2, R3, R4, R5, R6, R7, R8 and R9 are independently hydrogen, alkyl, alkenyl, aryl or aralkyl; or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring; and

[0007] (b) a lubricating oil.

[0008] The present invention is further directed to a method for improving the anti-wear characteristics of a lubricating oil by adding from 0.1% to 20% of a compound of formula I.

[0009] The present invention is further directed to a lubricating oil composition containing the reaction product of a compound of formula (I) with an imine; an unsaturated carboxylic acid or ester; an isocyanate or isothiocyanate; or an alkyl, alkenyl or aralkyl group bearing a leaving group; and to the aforementioned reaction products.

DETAILED DESCRIPTION

[0010] All percentages are weight percentages based on the entire composition described, unless specified otherwise. An “alkyl” group is a saturated hydrocarbyl group having from one to twenty-two carbon atoms in a linear, branched or cyclic arrangement, and having from 0 to 2 oxygen, nitrogen or sulfur atoms. Substitution on alkyl groups of one or more halo, hydroxy, alkoxy, alkanoyl or amido groups is permitted; alkoxy, alkanoyl and amido groups may in turn be substituted by one or more halo substituents. In one preferred embodiment, alkyl groups contain from two to twelve carbon atoms and from 0 to 1 oxygen, nitrogen or sulfur atoms; in another preferred embodiment, alkyl groups contain from 4 to 22 carbon atoms; in another preferred embodiment, alkyl groups contain no heteroatoms. An “alkenyl” group is an “alkyl” group in which at least one carbon-carbon single bond has been replaced with a double bond. An “aryl” group is a substituent derived from an aromatic compound, including heterocyclic aromatic compounds having heteroatoms chosen from among nitrogen, oxygen and sulfur. An aryl group has a total of from five to twenty ring atoms, and has one or more rings which are separate or fused. Substitution on aryl groups of one or more halo, alkyl, alkenyl, hydroxy, alkoxy, alkanoyl or amido groups is permitted, with substitution by one or more halo groups being possible on alkyl, alkenyl, alkoxy, alkanoyl or amido groups. An “aralkyl” group is an “alkyl” group substituted by an “aryl” group. A “lubricating oil” is a natural or synthetic oil, or a mixture thereof, having suitable viscosity for use as a lubricant, e.g., as crankcase oil in an internal combustion engine, automatic transmission fluid, turbine lubricant, gear lubricant, compressor lubricant, metal-working lubricant, hydraulic fluid, etc.

[0011] Preferably, at least one of R1, R2, R3, R4, R5, R6, R7, R8 and R9 is alkyl, alkenyl, aryl or aralkyl or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring; more preferably at least two of R1, R2, R3, R4, R5, R6, R7, R8 and R9 are alkyl, alkenyl, aryl or aralkyl. In one embodiment of the invention at least one of R1, R2, R3, R4, R5, R6, R7, R8 and R9 is aryl, aralkyl, C4-C22 alkyl or C4-C22 alkenyl; more preferably at least one of R1, R2, R3, R4, R5, R6, R7, R8 and R9 is C4-C22 alkyl or C4-C22 alkenyl; and most preferably at least one of R1, R2, R3, R4, R5, R6, R7, R8 and R9 is C6-C22 alkyl. The composition of the present invention includes at least one compound of formula (I). In one embodiment of the invention, the composition contains at least two compounds of formula (I), and more preferably contains at least three compounds of formula (I).

[0012] In one embodiment of the invention, R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring, preferably a C5-C8 alkyl or alkenyl ring, most preferably a C5-C6 alkyl ring. In this embodiment, either or both pairs of substituents, R1 and R2, or R3 and R4, become a difunctional alkyl or alkenyl group linked to the cyclic thioamide ring carbon to form an alkyl or alkenyl ring, resulting in a mono- or di-spiro-compound. For example, when X is CH2; and R1 and R2, and R3 and R4 combine with a ring carbon atom to form a C6 alkyl ring, the following structure results: 3

[0013] In one embodiment of the invention, X is CR5R6, and the compound of formula (I) can be represented by formula (II) 4

[0014] Preferably, at least one of R1, R2, R3, R4, R5 and R6 is alkyl, alkenyl, aryl or aralkyl, or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form a C5-C8 alkyl or alkenyl ring. In a preferred embodiment of the invention, R4 is R10NH, and R10 is alkyl, alkenyl, aryl or aralkyl. The compound of this embodiment can be prepared from an alkyl nitrile, a ketone bearing a leaving group at the α-position, and an amine, in a three-step process, as shown below in Scheme 1 for the embodiment in which R5 and R6 are hydrogen: 5

[0015] wherein Z represents a suitable leaving group, including, but not limited to iodide, bromide, chloride, tosylate, mesylate or triflate. Preferably, R3 is alkyl, alkenyl, aryl or aralkyl. Preferably, R1, R2 and R3 contain no amine nitrogen atoms. Preferably, at least one of R1, R2, R3 and R10 is aryl, aralkyl, C4-C22 alkyl or C4-C22 alkenyl; more preferably C6-C22 alkyl or C6-C22 alkenyl; and most preferably C10-C22 alkyl. Use of a more highly substituted ketone starting material will result in a product in which one or both of R5 and R6 are not hydrogen.

[0016] In one embodiment of the invention, a compound of formula (I) in which X is CH2 is prepared from a 1,2-halohydrin, an alkyl nitrile and a sulfide salt, in a two-step process, as shown below in Scheme 2: 6

[0017] wherein Z represents a suitable leaving group, including, but not limited to iodide, bromide, chloride, tosylate, mesylate or triflate. The process can also be performed with substituted starting material to produce a compound in which X is CR5R6, and R5 and R6 are not hydrogen.

[0018] In another embodiment of the invention, X is CR5R6CR8R9 and the compound of formula (I) can be represented by formula (III) 7

[0019] Preferably, at least one of R1, R2, R3, R4, R5, R6, R8 and R9 is alkyl, alkenyl, aryl or aralkyl, or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form a C5-C8 alkyl or alkenyl ring. In a preferred embodiment of the invention, R4 is R10NH, and R10 is alkyl, alkenyl, aryl or aralkyl. Preferably, R3is alkyl, alkenyl, aryl or aralkyl. Preferably, R3 contains no amine nitrogen atoms. Preferably, at least one of R3 and R4is aryl, aralkyl, C4-C22 alkyl or C4-C22 alkenyl; more preferably C6-C22 alkyl or alkenyl; and most preferably C10-C22 alkyl. In one embodiment of the invention, R1, R2, R5, R6, R8 and R9 are hydrogen, and the compound of formula (III) is prepared according to the following two-step process 8

[0020] This process also may be performed with various R groups on the starting material to give substituted versions of the product in which some or all of R1, R2, R5, R6, R8 and R9 are not hydrogen. The process also is capable of producing the five-membered analog of the product, i.e., X is CR5R6, with or without substituents on the ring carbons. This is illustrated below in Scheme 4 for the embodiment in which R1, R2, R5 and R6 are hydrogen: 9

[0021] In another embodiment of the invention, X is CR5R6NR7 and the compound of formula (I) can be represented by formula (IV) 10

[0022] Preferably, at least one of R1, R2, R3, R4, R5, R6 and R7 is alkyl, alkenyl, aryl or aralkyl, or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form a C5-C8 alkyl or alkenyl ring. In a preferred embodiment, R1, R2, R5, R6 and R7 are hydrogen, and the compound of formula (IV) is prepared according to the following two-step process 11

[0023] This process also may be performed with various R groups on the starting material, or with subsequent alkylation on the amine nitrogen, to give substituted versions of the product in which some or all of R1, R2, R5, R6 and R7 are not hydrogen. Preferably, at least one of R3 and R4 is alkyl, alkenyl, aryl or aralkyl; more preferably at least one of R3 and R4 is aryl, aralkyl, C4-C22 alkyl or C4-C22 alkenyl; more preferably C6-C22 alkyl or C6-C22 alkenyl; and most preferably C10-C22 alkyl. Preferably, R3 and R4 contain no amine nitrogen atoms.

[0024] In a preferred embodiment of the invention, the thioamide group or an amine group of the compound of formula (I) is further functionalized by reaction with imines of formula R11N═CR12R13; unsaturated carboxylic esters of formula CHR14═CR15COOR16; isocyanates, R18NCO, or isothiocyanates, R18NCS; or R17Y; wherein R12, R13 and R16 independently are hydrogen, alkyl, alkenyl, aryl or aralkyl; R17 is alkyl, alkenyl or aralkyl; R14 and R15 independently are hydrogen or C1-C4 alkyl; R11 and R18 independently are alkyl, alkenyl, aryl or aralkyl; and Y is a suitable leaving group capable of being displaced by the nitrogen or the sulfur of a thioamide group, or by a primary or secondary amine nitrogen. Suitable leaving groups include, e.g., iodide, bromide, chloride, tosylate, mesylate or triflate. Functionalization of the thioamide group can occur on the thioamide nitrogen or the thioamide sulfur, provided of course that the thioamide nitrogen bears at least one hydrogen. The product also can be a mixture of the compound functionalized on the nitrogen and the one functionalized on the sulfur. In compounds also having a primary or secondary amino group, functionalization also may occur solely or partially on the amino group.

[0025] Preferably, R14 and R15 independently are hydrogen or methyl. Preferably, the compound of formula CHR14═CR15COOR16 is an alkyl or aralkyl acrylate having R14=R15=H and R16=alkyl or aralkyl; or a methacrylate ester having R14=H and R15=CH3; or a crotonate ester having R15=H and R14=CH3. Preferably, R14 is hydrogen. Preferably, R16 is alkyl or aralkyl, most preferably C4-C22 alkyl. Preferably, R18 is aryl, alkyl or aralkyl, most preferably C8-C22 alkyl. Preferably, R11 is C12-C22 alkyl. In one embodiment, R11 is derived from an unsubstituted C16-C22 alkyl amine, R11NH2, preferably one which is an oil-soluble amine. In one embodiment, the alkyl amine is a tertiary alkyl primary amine, i.e., a primary amine in which the alkyl group is attached to the amino group through a tertiary carbon. Examples of commercially available tertiary alkyl primary amines are the Primene™ amines available from Rohm and Haas Company, Philadelphia, Pa. Preferably, R12 and R13 independently are alkyl or hydrogen. In a preferred embodiment of the invention, R11N═CR12R13 is a formaldehyde imine, R11N=CH2. Preferably, R17 is C4-C22 alkyl, C4-C22 alkenyl or aralkyl; more preferably C6-C22 alkyl or C6-C22 alkenyl; and most preferably C8-C22 alkyl.

[0026] As an example, the reaction of the compound of formula (II) with an imine and an acrylate is illustrated below in Scheme 6. 12

[0027] The compound resulting from functionalization of the thioamide group in the compound of formula (II) can be represented by formula (V). 13

[0028] wherein bonds a and b are single or double bonds, provided that one of a and b is a single bond and the other is a double bond; one of B1 and B2 is —CR14H—CR15H—COOR16, —CR12R13NHR11, —C(O)NHR18, —C(S)NHR18 or R17, and the other is absent. When B1 is present, bond “b” is a double bond; and when B2 is present, bond “a” is a double bond. An analogous structure exists for the compound resulting from functionalization of the compound of formula (III), in which functionalization also occurs on the thioamide nitrogen or sulfur, as shown in formula (VI). 14

[0029] The compound resulting from functionalization of the thioamide group and/or a secondary amino group in the compound of formula (IV) can be represented by formula (VII). 15

[0030] wherein B3 represents R7, —CR14H—CR15H—COOR16, —CR12R13NHR11, —C(O)NHR18, —C(S)NHR18 or R17. If R7 in formula (IV) is not hydrogen, then functionalization at the NR7amino group would not occur, and B3 would simply be R7. Other primary or secondary amino groups in formulas (II), (III) or (IV) can be functionalized in this way, e.g., when R4 is R10NH, the R10NH amino group can be functionalized.

[0031] Preferably, the compound(s) of formula (I) is present in a lubricating oil in a total amount of at least 0.2%, more preferably at least 0.3%, and most preferably at least 0.4%. Preferably, the compound(s) of formula (I) is present in a lubricating oil in a total amount no greater than 10%, more preferably no greater than 5%, and most preferably no greater than 2%. Preferably, the compounds are soluble at the aforementioned levels.

[0032] Optionally, other additives typically used in lubricating oils are present in the composition. Such additives include, but are not limited to, other anti-wear additives, anti-corrosion additives, dispersants, detergents, antioxidants, antifoamants, friction modifiers, seal swell agents, demulsifiers, viscosity index improvers and pour point depressants. Other anti-wear additives that can be used in combination with the compound of formula (I) include the commercial products known as ZDDP, which are zinc dialkyldithiophosphates. In addition to improving the anti-wear characteristics of lubricating oils, the compound of formula (I) typically also improves anti-corrosion characteristics and functions as an anti-oxidant.

Claims

1. A composition comprising: (a) from 0.1% to 20% of at least one cyclic thioamide of formula I: 16 wherein X is CR5R6, CR5R6NR7 or CR5R6CR8R9; R1, R2, R3, R4, R5, R6, R7, R8 and R9 are independently hydrogen, alkyl, alkenyl, aryl or aralkyl; or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form an alkyl or alkenyl ring; and (b) a lubricating oil.

2. The composition of claim 1 in which X is CR5R6, and at least one of R1, R2, R3, R4, R5 and R6 is alkyl, alkenyl, aryl or aralkyl, or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form a C5-C8 alkyl or alkenyl ring.

3. The composition of claim 2 in which R4 is R10NH, and R10 is alkyl, alkenyl, aryl or aralkyl.

4. The composition of claim 1 in which X is CR5R6CR8R9, and at least one of R1, R2, R3, R4, R5, R6, R8 and R9 is alkyl, alkenyl, aryl or aralkyl, or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form a C5-C8 alkyl or alkenyl ring.

5. The composition of claim 4 in which R4 is R10NH, and R10 is alkyl, alkenyl, aryl or aralkyl.

6. The composition of claim 1 in which X is CR5R6NR7, and at least one of R1, R2, R3, R4, R5 and R6 is alkyl, alkenyl, aryl or aralkyl, or R1 and R2, or R3 and R4, combine with the carbon atom to which they are attached to form a C5-C8 alkyl or alkenyl ring.

7. The composition of claim 6 in which R7 is hydrogen, and at least one of R3 and R4 is alkyl, alkenyl, aryl or aralkyl.

8. The composition of claim 1 in which at least one of R1, R2, R3, R4, R5, R6, R7, R8 and R9 is aryl, aralkyl, C4-C22 alkyl or C4-C22 alkenyl.

9. The composition of claim 1 which comprises at least two cyclic thioamide compounds of formula (I).

10. The method of claim 9 in which said at least two cyclic thioamide compounds are present in a total amount from 0.2% to 5%.