GB948201A - Condensation product of a phenol and an unsaturated hydrocarbon - Google Patents

Condensation product of a phenol and an unsaturated hydrocarbon

Info

Publication number
GB948201A
GB948201A GB2914461A GB2914461A GB948201A GB 948201 A GB948201 A GB 948201A GB 2914461 A GB2914461 A GB 2914461A GB 2914461 A GB2914461 A GB 2914461A GB 948201 A GB948201 A GB 948201A
Authority
GB
United Kingdom
Prior art keywords
phenol
benzene
dipb
condensate
solution
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
GB2914461A
Inventor
Laurence Faye Sonnabend
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.)
Dow Chemical Co
Original Assignee
Dow Chemical 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
Priority to NL268328D priority Critical patent/NL268328A/xx
Priority to US796276A priority patent/US3004953A/en
Application filed by Dow Chemical Co filed Critical Dow Chemical Co
Priority to GB2914461A priority patent/GB948201A/en
Publication of GB948201A publication Critical patent/GB948201A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/02Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Meta or para-diisopropenyl benzene or a mixture thereof is condensed with phenols at elevated temperatures in the presence of acidic alkylation catalysts. The phenol may be phenol itself, a bisphenol, or their alkylated derivatives having 1-4 carbon atoms per alkyl group, p-cresol, phenol, and bisphenol A being preferred. The diisopropenyl benzenes preferably accounts for 44-56 mole per cent. of the reactants. 0.8 to 1.25 mole of phenol per mole of diisopropenyl benzene are preferred, but excess phenol may be present. A solvent, e.g. aromatic hydrocarbons may be present. 60-125 DEG C. is preferred and the preferred catalysts are mineral acids e.g. sulphuric, these being usually 0.25-1% by weight of reactants. Reaction generally takes 2-6 hours, when the catalyst is normally neutralized with NaOH and volatiles are removed under vacuum. Films may be formed from solutions of the product in e.g. benzene or methyl ethyl ketone.ALSO:Condensates prepared from diisopropenyl benzene (DIPB), and phenols are used to make films on glass slides as follows: Example 1-50% solution in methyl ethyl ketone of p-cresol-p-DIPB condensate; Example 2-50% solution in benzene of phenol-p-DIPB condensate; Example 3-50% solution in benzene of phenol-m-DIPB condensate; Example 4-50% benzene solution of bisphenol A-p-DIPB condensate; Example 5-50% benzene solution of phenol-p-DIPB condensate; Example 6-as in 5 using m-DIPB; these solutions were cast on to microscope slides and dried at room temperature.
GB2914461A 1959-03-02 1961-08-11 Condensation product of a phenol and an unsaturated hydrocarbon Expired GB948201A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
NL268328D NL268328A (en) 1961-08-11
US796276A US3004953A (en) 1959-03-02 1959-03-02 Reaction products of phenols and diisopropenylbenzene
GB2914461A GB948201A (en) 1961-08-11 1961-08-11 Condensation product of a phenol and an unsaturated hydrocarbon

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2914461A GB948201A (en) 1961-08-11 1961-08-11 Condensation product of a phenol and an unsaturated hydrocarbon

Publications (1)

Publication Number Publication Date
GB948201A true GB948201A (en) 1964-01-29

Family

ID=10286849

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2914461A Expired GB948201A (en) 1959-03-02 1961-08-11 Condensation product of a phenol and an unsaturated hydrocarbon

Country Status (2)

Country Link
GB (1) GB948201A (en)
NL (1) NL268328A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115087683A (en) * 2020-02-07 2022-09-20 莱恩卡本德国有限公司 Novel tackifier for elastomer compound

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115087683A (en) * 2020-02-07 2022-09-20 莱恩卡本德国有限公司 Novel tackifier for elastomer compound
US11873366B2 (en) 2020-02-07 2024-01-16 Rain Carbon Germany Gmbh Tackifier for elastomer compounds
CN115087683B (en) * 2020-02-07 2024-05-03 莱恩卡本德国有限公司 Novel tackifier for elastomer compound

Also Published As

Publication number Publication date
NL268328A (en)

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