GB948201A - Condensation product of a phenol and an unsaturated hydrocarbon - Google Patents
Condensation product of a phenol and an unsaturated hydrocarbonInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular 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.
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)
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 |
-
0
- NL NL268328D patent/NL268328A/xx unknown
-
1961
- 1961-08-11 GB GB2914461A patent/GB948201A/en not_active Expired
Cited By (3)
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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