JPS55145626A - New phenol derivative - Google Patents
New phenol derivativeInfo
- Publication number
- JPS55145626A JPS55145626A JP5201179A JP5201179A JPS55145626A JP S55145626 A JPS55145626 A JP S55145626A JP 5201179 A JP5201179 A JP 5201179A JP 5201179 A JP5201179 A JP 5201179A JP S55145626 A JPS55145626 A JP S55145626A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- formual
- phenol
- phenol derivative
- compound
- 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.)
- Granted
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
NEW MATERIAL:Phenol derivative of formula I (n is 4W16; m is 1W2).
EXAMPLE: 2-[2-Methyl-2-(2-hydroxyphenyl)ethyl]-4-nonylphenol.
USE: Raw material of phenolic resin, etc. having large void volume in the network structure compared with conventional phenolic resins and having an elasticity ascribed to intramolecular plasticization effect of alkyl group. Flexibility and processability of resins can be improved.
PROCESS: For example, a compound of formula I is obtained by reacting phenol with an allylalkylphenol of formula II or a diallylalkylphenol of formual III at 50W 200°C for 1W10hr in the presence of an acid catalyst such as AlCl3. The molar ratio of phenol and the compound of formual II or formual III is 1:1W0.01.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5201179A JPS55145626A (en) | 1979-04-28 | 1979-04-28 | New phenol derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5201179A JPS55145626A (en) | 1979-04-28 | 1979-04-28 | New phenol derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS55145626A true JPS55145626A (en) | 1980-11-13 |
JPS6313974B2 JPS6313974B2 (en) | 1988-03-29 |
Family
ID=12902866
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5201179A Granted JPS55145626A (en) | 1979-04-28 | 1979-04-28 | New phenol derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55145626A (en) |
-
1979
- 1979-04-28 JP JP5201179A patent/JPS55145626A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6313974B2 (en) | 1988-03-29 |
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