IP Library Granted Patent US 10,829,436
Granted Patent B2
US 10,829,436 · App. 16/493,830 · Granted Nov 10, 2020

Ester compounds, method for the production thereof and use thereof

Inventors: Tobias Betke (Bielefeld, DE); Carmen Plass (Bielefeld, DE); Harald Gröger (Bielefeld, DE); Dirk Loderer (Munich, DE); Stefan Seemeyer (Munich, DE); Thomas Kilthau (Munich, DE); Ling Ma (Munich, DE)
Assignees: Klüber Lubrication München SE & CO. KG; Universität Bielefeld
C07C69/67C07C67/02C10M105/42C12P7/62C10M2207/301C10N2070/00
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 10,829,436
App. No.
16/493,830
Granted
Nov 10, 2020
Kind
B2
Abstract

The invention relates to novel ester compounds of the general formula (I) to a process for preparation thereof and to the use thereof. These ester compounds may contain a mixture of at least two compounds of the general formula (I).

Claims (53)

1. A lubricant composition for the lubrication of machinery, comprising:

a mixture of at least two ester compounds of the general formulae (I)

in which

the A radical is selected from the group consisting of CH 2 , CH 2 CH 2 , cis-CH═CH and/or trans-CH═CH,

n is 0 or 1 to 20,

m is 1 to 20,

the R 1 radical is selected from the group consisting of hydrogen, branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 2 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals, C 1 - to C 60 -heteroarylalkyl radicals, C 6 - to C 60 -aryl radicals, and/or cyclically saturated or unsaturated C 5 - to C 60 -alkyl radicals, where these are unsubstituted or mono- or polysubstituted by at least one substituent selected from the group of OH, R 4 , R 5 , O-acetyl,

the R 2 radical is selected from the group consisting of H, branched or unbranched C 2 - to C 60 -alkyl radicals, C 2 - to C 60 -heteroalkyl radicals, C 7 - to C 60 -arylalkyl radicals, C 6 - to C 60 -heteroarylalkyl radicals, C 6 - to C 60 -aryl radicals, and/or cyclically saturated or unsaturated C 5 - to C 60 -alkyl radicals, where these are unsubstituted or mono- or polysubstituted by at least one substituent selected from the group of OH, O—C(O)—R 1 , CH 2 OH, CO 2 H, CO 2 R 1 , R 5 , and also branched or unbranched C 2 - to C 60 -alkenyl radicals or methyl, where this is unsubstituted or mono- or polysubstituted by at least one substituent selected from the group of OH, O—C(O)—R 1 , CH 2 OH, CO 2 H, CO 2 R 1 , R 5 ,

the R 3 radical is selected from the group consisting of branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 2 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals and/or C 6 - to C 60 -heteroarylalkyl radicals, where these are unsubstituted or mono- or polysubstituted by at least one substituent selected from the group of OH, CH 2 OH, CH 2 —R 4 ,

the R 4 radical has the following structure (II):

in which the R 2 , R 3 and A radicals and the numbers m and n present therein are defined as described above,

the R 5 radical has the following structure (III):

in which the R 1 , R 3 and A radicals and the numbers m and n present therein are defined as described above; and

one or more anticorrosion additives, antioxidants, antiwear additives, UV stabilizers, inorganic or organic solid lubricants, pour point and viscosity index improvers, adhesion additives, dyes, emulsifiers, and defoamers.

2. A method comprising:

providing a lubricant composition according to claim 1 ; and

applying the lubricant composition for lubrication of machinery in the marine sector, for lubrication of machinery in the food processing industry, for lubrication of ball bearings and slide bearings, for lubrication of transport and control chains in vehicle technology, for lubrication in conveying technology, for lubrication in mechanical engineering, for lubrication in office technology, for lubrication of bevel gears and spur gears, for lubrication of roller bearings in continuous casting plants and transport bearings in continuous kilns, or for open crown gear lubrication in rotary kilns, tubular mills, drums and mixers in the cement, lime, gypsum, mining and chemical industries.

3. The lubricant composition as claimed in claim 1 wherein each of the ester compounds in the mixture of at least two ester compounds of the general formulae (I) has the general structure of one or more of:

the general structure (Ia)

in which

n′ and n″ are either 1 and 2 or 2 and 1,

m′ is 1 to 5,

the R 1 radical is selected from the group consisting of hydrogen, branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 2 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals, C 1 - to C 60 -heteroarylalkyl radicals and/or C 6 - to C 60 -aryl radicals,

the R 2 radical is selected from the group consisting of branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 2 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals and/or C 6 - to C 60 -heteroarylalkyl radicals and/or cyclically saturated and or unsaturated C 5 - to C 60 -alkyl radicals, where these are unsubstituted or mono- or polysubstituted by at least one substituent selected from the group of OH, CH 2 OH;

the general structure (Ib)

in which

n′ and n″ are either 1 and 2 or 2 and 1, n′″ is 0 to 10,

m′ is 1 to 5,

the R 2 radical is selected from the group consisting of branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 1 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals and/or C 6 - to C 60 -heteroarylalkyl radicals and/or cyclically saturated and or unsaturated C 5 - to C 60 -alkyl radicals, where these are unsubstituted or mono- or polysubstituted by at least one substituent selected from the group of OH, CH 2 OH,

R 6 radical is selected from the group consisting of branched or unbranched C 1 - to C 60 -alkyl radicals and branched or unbranched C 2 - to C 60 -alkenyl radicals; and

the general structure (Ic)

in which

n′ and n″ are either 1 and 2 or 2 and 1, n′″ is 0 to 10,

m′ is 1 to 5,

the R 1 radical is selected from the group consisting of hydrogen, branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 1 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals, C 1 - to C 60 -heteroarylalkyl radicals and/or C 6 - to C 60 -aryl radicals,

the R 6 radical is selected from the group consisting of branched or unbranched C 1 - to C 60 -alkyl radicals and branched or unbranched C 2 - to C 60 -alkenyl radicals.

4. The lubricant composition of claim 1 , further comprising at least one further base oil component.

5. The lubricant composition of claim 4 , wherein the at least one further base oil component is selected from the group consisting of natural glyceride esters, natural fatty acids, sunflower oil, rapeseed oil, colza oil, linseed oil, corn oil, corn germ oil, safflower oil, soybean oil, linseed oil, groundnut oil, lesquerella oil, palm oil, and olive oil, ethers, polyether polyols and perfluoropolyethers, alkyl diphenyl ethers and polyphenyl ethers, silicone oils, polyglycols consisting of randomly distributed polyoxyethylene and/or polyoxypropylene units and/or other polyoxyalkylene units, and other glycol derivatives, polyalphaolefins including those prepared by metallocene catalysis, and alpha-olefin copolymers, polymeric systems, unhydrogenated, partly hydrogenated or fully hydrogenated polyisobutylene or a mixture thereof, styrene and polystyrene and their derivatives and/or polymeric systems based on acrylates, acetate polymers and amides, polyethylenes, polypropylenes, halogenated polypropylenes and/or cycloalkanes, mineral oils, white oil, alkylated diphenyl ethers, alkylated naphthalenes and perfluoropolyethers, and mixtures thereof.

6. The lubricant composition of claim 1 , further comprising at least one further ester not having the general formula (I).

7. The lubricant composition of claim 6 , wherein the at least one further ester is selected from the group consisting of trimethylolpropane and pentaerythritol esters, TMP complex esters in fully or partly esterified form with saturated and/or mono- or polyunsaturated carboxylic acids of chain length C6-C36, where these may be linear or branched, complex esters of dimer acids, dimer acid esters, ethylhexyl dimerate, aliphatic carboxylic, dicarboxylic esters, phosphate esters, trimellitic and pyromellitic esters, and natural glyceride ester.

8. The lubricant composition of claim 1 , further comprising a thickener.

9. The lubricant composition as claimed in claim 1 wherein each of the ester compounds in the mixture of at least two ester compounds of the general formulae (I) has the general structure (Ia)

in which

n′ and n″ are either 1 and 2 or 2 and 1,

m′ is 1 to 5,

the R 1 radical is selected from the group consisting of hydrogen, branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 2 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals, C 1 - to C 60 -heteroarylalkyl radicals and/or C 6 - to C 60 -aryl radicals,

the R 2 radical is selected from the group consisting of branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 2 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals and/or C 6 - to C 60 -heteroarylalkyl radicals and/or cyclically saturated and or unsaturated C 5 - to C 60 -alkyl radicals, where these are unsubstituted or mono- or polysubstituted by at least one substituent selected from the group of OH, CH 2 OH.

10. The lubricant composition-as claimed in claim 1 wherein each of the ester compounds in the mixture of at least two ester compounds of the general formulae (I) has the general structure (Ib)

in which

n′ and n″ are either 1 and 2 or 2 and 1, n′″ is 0 to 10,

m′ is 1 to 5,

the R 2 radical is selected from the group consisting of branched or unbranched C 1 - to C 60 -alkyl radicals, branched or unbranched C 1 - to C 60 -alkenyl radicals, C 7 - to C 60 -arylalkyl radicals and/or C 6 - to C 60 -heteroarylalkyl radicals and/or cyclically saturated and or unsaturated C 5 - to C 60 -alkyl radicals, where these are unsubstituted or mono- or polysubstituted by at least one substituent selected from the group of OH, CH 2 OH,

R 6 radical is selected from the group consisting of branched or unbranched C 1 - to C 60 -alkyl radicals and branched or unbranched C 2 - to C 60 -alkenyl radicals.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2019
From: BETKE, TOBIAS; PLASS, CARMEN; GRÖGER, HARALD; LODERER, DIRK; SEEMEYER, STEFAN; KILTHAU, THOMAS; MA, LING
To: KLÜBER LUBRICATION MÜNCHEN SE & CO. KG; UNIVERSITÄTSSTR BIELEFELD
Reel/Frame 050730/0516 →
Priority Claims (2)
DE 10 2017 003 647 · Apr 13, 2017 · national
DE 10 2018 002 891 · Apr 10, 2018 · national
Continuity (1)
Related Publication 20200140370A1 · May 7, 2020