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 rubber

Info

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
Application number
GB3598057A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bridgestone Firestone Inc
Original Assignee
Firestone Tire and Rubber Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Firestone Tire and Rubber Co filed Critical Firestone Tire and Rubber Co
Priority to GB3598057A priority Critical patent/GB835826A/en
Publication of GB835826A publication Critical patent/GB835826A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/17Amines; Quaternary ammonium compounds
    • C08K5/19Quaternary ammonium compounds

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  • 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.
GB3598057A 1957-11-19 1957-11-19 Improvements relating to reaction products of hydrocarbon dihalides and substituted phenylenediamines and their use in rubber Expired GB835826A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (23)

* Cited by examiner, † Cited by third party
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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