GB835826A - Improvements relating to reaction products of hydrocarbon dihalides and substituted phenylenediamines and their use in rubber - Google Patents
Improvements relating to reaction products of hydrocarbon dihalides and substituted phenylenediamines and their use in rubberInfo
- Publication number
- GB835826A GB835826A GB3598057A GB3598057A GB835826A GB 835826 A GB835826 A GB 835826A GB 3598057 A GB3598057 A GB 3598057A GB 3598057 A GB3598057 A GB 3598057A GB 835826 A GB835826 A GB 835826A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- hydrogen
- dimethyl
- phenylenediamine
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/19—Quaternary ammonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyamides (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises the reaction product of a C1-C8 hydrocarbon dihalide where the halogen is chlorine, bromine or iodine and a substituted phenylenediamine of the formula R1R2NC6H4NHR3, in which R1, R2 and R3 are C1-C20 alkyl, cycloalkyl, alkylcycloalkyl or hydroxyalkyl groups, R2 may be hydrogen, and R1 and R2 may be joined as a C2-C10 alkylene group, and the phenylenediamine is the ortho or para isomer. The products may be of the following general formulae <FORM:0835826/IV (b)/1> <FORM:0835826/IV (b)/2> <FORM:0835826/IV (b)/3> where X is chlorine, bromine or iodine, and R's are as above. o- and p-Phenylenediamines which may be used in the preparation of the above compounds are the N,N1 dimethyl, diethyl, dipropyl, dibutyl, dioctyl and dicyclohexyl, N-methyl, N1-ethyl; N-ethyl, N1-butyl; N-methyl, N1-cyclohexyl; N,N-dimethyl-N1-hexyl; N,N - dimethyl - N1 - eicosyl; N,N1-dimethyl - N1 - undecyl; N,N - di - n - propyl-N1 - cyclohexyl; N,N1 - dimethyl - N1 - ethyl; N,N1 - dicyclohexyl N1 - methyl; N,N1 - di-amyl - N1 - octyl; N - methyl - N - ethyl, N1-isopropyl; N,N - dibutyl - N1 - sec. butyl; N,N - diethyl - N1 - sec. butyl; N,N1 - ethy-lene - N1 - (4 - hydroxy - 4 - methyl - 2 - hexyl); and N,N1 - (gamma - iso - amylpentamethylene) N1 - iso - propyl compounds. The last but one of the above compounds may be prepared by reacting ethylene dibromide with p-nitraniline and reducing the resulting condensate with iron and hydrochloric acid. The N,N-ethylene p-phenylenediamine so formed is then alkylated with 4 - hydroxy - 4 - methyl - 2 - pentanone, in ethanol and glacial acetic acid in the presence of Adam's platinum oxide catalyst, under hydrogen. The last of the above compounds may be prepared by condensing gamma picoline with i-butyraldehyde, and reducing the condensate with hydrogen and a nickel catalyst. The gamma-i-amylpiperidine so formed is then condensed with p-nitrochloro benzene, the condensate reduced with iron and hydrochloric acid, and the resulting N,N (gamma-i-amylpentamethylene) - p - phenylene diamine alkylated with acetone in the presence of hydrogen and Adam's catalyst. The other phenylenediamines mentioned are prepared from the appropriate N,N1 disubstituted phenylenediamine by reaction with the appropriate ketone in the presence of hydrogen and the platinum catalyst. Suitable hydrocarbon dihalides specified are methylene, propylene, butylene, tetramethylene, pentylene, hexamethylene, hexylene, octylene, methylethylene, pentamethylene and styrene dichloride and dibromide, ethylene, dichloride, dibromide, and diiodide, trimethylene dichloride, dibromide and bromoiodide, 1-chloro-2-bromoethane, 1,2, dibromocyclohexane, 1,2, and 1,3, dibromobutane; 1,4-dichlorobutene-2. Examples are given.ALSO:Compositions are described of a sulphur vulcanized rubber composition with an antiozone agent prepared by the condensation of a C1-C8 hydrocarbon dihalide with a substituted o- or p-phenylenediamine of formula R1R2NC6H4NHR3 where R1, R2 and R3 are alkyl, cycloalkyl, alkyl cycloalkyl, or hydroxyalkyl groups of 1-20 carbon atoms, R2 may also be hydrogen, and R1 and R2 may be joined as an alkylene group containing 2-10 carbon atoms. Halogens specified are chlorine, bromine and iodine. The rubbers used may be natural rubber, a polymer of butadiene or an alkyl derivative thereof, a copolymer of butadiene or an alkyl derivative thereof with a vinyl monomer, e.g. GR-S, or a mixture of any of these rubbers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3598057A GB835826A (en) | 1957-11-19 | 1957-11-19 | Improvements relating to reaction products of hydrocarbon dihalides and substituted phenylenediamines and their use in rubber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3598057A GB835826A (en) | 1957-11-19 | 1957-11-19 | Improvements relating to reaction products of hydrocarbon dihalides and substituted phenylenediamines and their use in rubber |
Publications (1)
Publication Number | Publication Date |
---|---|
GB835826A true GB835826A (en) | 1960-05-25 |
Family
ID=10383633
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3598057A Expired GB835826A (en) | 1957-11-19 | 1957-11-19 | Improvements relating to reaction products of hydrocarbon dihalides and substituted phenylenediamines and their use in rubber |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB835826A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009076090A2 (en) * | 2007-12-12 | 2009-06-18 | Chemtura Corporation | Cycloalkyl phenylenediamines as deposit control agents for lubricants |
WO2013090051A1 (en) | 2011-12-13 | 2013-06-20 | Chemtura Corporation | Cross products and co-oligomers of phenylenediamines and aromatic amines as antioxidants for lubricants |
US8563489B2 (en) | 2007-12-12 | 2013-10-22 | Chemtura Corporation | Alkylated 1,3-benzenediamine compounds and methods for producing same |
JP2015221856A (en) * | 2014-05-22 | 2015-12-10 | 株式会社ブリヂストン | Rubber composition, tire, bisphenyl diamine compound and anti-aging agent |
WO2018013181A1 (en) | 2016-07-13 | 2018-01-18 | Chevron Oronite Company Llc | Synergistic lubricating oil composition containing mixture of antioxidants |
US10160845B2 (en) * | 2015-12-22 | 2018-12-25 | Eastman Chemical Company | Methods of making compounds and mixtures having antidegradant and antifatigue efficacy |
US10160718B2 (en) | 2015-12-22 | 2018-12-25 | Eastman Chemical Company | Methods of making compounds having antidegradant and antifatigue efficacy |
US10167252B2 (en) * | 2015-12-22 | 2019-01-01 | Eastman Chemical Company | Compounds and mixtures with antidegradant and antifatigue efficacy and compositions including such compounds |
US10260017B2 (en) * | 2015-12-22 | 2019-04-16 | Eastman Chemical Company | Compounds and mixtures with antidegradant and antifatigue efficacy and compositions including said compounds |
US10428009B2 (en) | 2015-12-22 | 2019-10-01 | Eastman Chemical Company | Methods of making compounds and mixtures having antidegradant and antifatigue efficacy |
CN110691769A (en) * | 2017-06-09 | 2020-01-14 | 伊士曼化工公司 | Compounds and mixtures having antidegradants and antifatigue efficacy and compositions comprising said compounds |
-
1957
- 1957-11-19 GB GB3598057A patent/GB835826A/en not_active Expired
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009076090A3 (en) * | 2007-12-12 | 2010-03-11 | Chemtura Corporation | Cycloalkyl phenylenediamines as deposit control agents for lubricants |
JP2011506452A (en) * | 2007-12-12 | 2011-03-03 | ケムチュア コーポレイション | Cycloalkylphenylenediamines as deposit control agents for lubricating oils. |
US8563489B2 (en) | 2007-12-12 | 2013-10-22 | Chemtura Corporation | Alkylated 1,3-benzenediamine compounds and methods for producing same |
WO2009076090A2 (en) * | 2007-12-12 | 2009-06-18 | Chemtura Corporation | Cycloalkyl phenylenediamines as deposit control agents for lubricants |
WO2013090051A1 (en) | 2011-12-13 | 2013-06-20 | Chemtura Corporation | Cross products and co-oligomers of phenylenediamines and aromatic amines as antioxidants for lubricants |
CN106459500B (en) * | 2014-05-22 | 2018-08-03 | 大塚化学株式会社 | Rubber composition, tire, double phenylenediamine compounds and age resister |
JP2015221856A (en) * | 2014-05-22 | 2015-12-10 | 株式会社ブリヂストン | Rubber composition, tire, bisphenyl diamine compound and anti-aging agent |
CN106459500A (en) * | 2014-05-22 | 2017-02-22 | 大塚化学株式会社 | Rubber composition, tire, bisphenyl diamine compound and anti-aging agent |
US10011704B2 (en) | 2014-05-22 | 2018-07-03 | Otsuka Chemical Co., Ltd. | Rubber composition, tire, bisphenyldiamine compound, and anti-aging agent |
US10260017B2 (en) * | 2015-12-22 | 2019-04-16 | Eastman Chemical Company | Compounds and mixtures with antidegradant and antifatigue efficacy and compositions including said compounds |
US10287418B2 (en) * | 2015-12-22 | 2019-05-14 | Eastman Chemical Company | Compounds with antidegradant and antifatigue efficacy and compositions including said compounds |
US10160845B2 (en) * | 2015-12-22 | 2018-12-25 | Eastman Chemical Company | Methods of making compounds and mixtures having antidegradant and antifatigue efficacy |
US10160718B2 (en) | 2015-12-22 | 2018-12-25 | Eastman Chemical Company | Methods of making compounds having antidegradant and antifatigue efficacy |
US10167252B2 (en) * | 2015-12-22 | 2019-01-01 | Eastman Chemical Company | Compounds and mixtures with antidegradant and antifatigue efficacy and compositions including such compounds |
JP2019506373A (en) * | 2015-12-22 | 2019-03-07 | イーストマン ケミカル カンパニー | Compounds having anti-degradation and anti-fatigue effects and compositions comprising said compounds |
JP2021001335A (en) * | 2015-12-22 | 2021-01-07 | イーストマン ケミカル カンパニー | Compounds with antidegradant and antifatigue efficacy and compositions including those compounds |
US10611719B2 (en) | 2015-12-22 | 2020-04-07 | Eastman Chemical Company | Methods of making compounds and mixtures having antidegradant and antifatigue efficacy |
US10407562B2 (en) | 2015-12-22 | 2019-09-10 | Eastman Chemical Company | Compounds with antidegradant and antifatigue efficacy and compositions including said compounds |
US10428009B2 (en) | 2015-12-22 | 2019-10-01 | Eastman Chemical Company | Methods of making compounds and mixtures having antidegradant and antifatigue efficacy |
US10077410B2 (en) | 2016-07-13 | 2018-09-18 | Chevron Oronite Company Llc | Synergistic lubricating oil composition containing mixture of antioxidants |
WO2018013181A1 (en) | 2016-07-13 | 2018-01-18 | Chevron Oronite Company Llc | Synergistic lubricating oil composition containing mixture of antioxidants |
CN110691769A (en) * | 2017-06-09 | 2020-01-14 | 伊士曼化工公司 | Compounds and mixtures having antidegradants and antifatigue efficacy and compositions comprising said compounds |
CN110691769B (en) * | 2017-06-09 | 2023-03-10 | 伊士曼化工公司 | Compounds and mixtures having antidegradants and antifatigue efficacy and compositions comprising said compounds |
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