JPS5564537A - Preparation of bis (3,5-dihydroxymethyl-4-hydroxyphenyl) alkane - Google Patents
Preparation of bis (3,5-dihydroxymethyl-4-hydroxyphenyl) alkaneInfo
- Publication number
- JPS5564537A JPS5564537A JP13668478A JP13668478A JPS5564537A JP S5564537 A JPS5564537 A JP S5564537A JP 13668478 A JP13668478 A JP 13668478A JP 13668478 A JP13668478 A JP 13668478A JP S5564537 A JPS5564537 A JP S5564537A
- Authority
- JP
- Japan
- Prior art keywords
- bis
- hydroxyphenyl
- alkane
- dihydroxymethyl
- formaldehyde
- 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
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
PURPOSE: To prepare a crystallized bis(3,5-dihydroxymethyl-4-hydroxyphenyl) alkane having high quality and useful as a raw material of epoxy resins, etc., by reacting a bis(4-hydroxy-phenyl)alkane with formaldehyde in the presence of a basic catalyst under specific conditions and thereafter precipitating the product with acid.
CONSTITUTION: (A) 1mol of a bis(4-hydroxyphenyl)alkane selected from bis (4-hydroxyphenyl)methane, 1, 1-bis(4-hydroxyphenyl)ethane and 2,2-bis(4-hydroxyphenyl)propane is reacted with (B) 3.7W4.3mol of formaldehyde in an aqueous solution at 0W55°C, preferably at 30W50°C in the presence of a strong base catalyst containing 1.6W2.5gram atom of an alkali metal, e.g. sodium hydroxide, etc. The product is precipitated with a diluted hydrochloric acid, etc. at 0W40°C to give the desired compound.
USE: Additives for novolak-phenol resins, curing agents for epoxy resins, etc.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53136684A JPS599534B2 (en) | 1978-11-08 | 1978-11-08 | Method for producing bis(3,5-dihydroxymethyl-4-hydroxyphenyl) alkanes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53136684A JPS599534B2 (en) | 1978-11-08 | 1978-11-08 | Method for producing bis(3,5-dihydroxymethyl-4-hydroxyphenyl) alkanes |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5564537A true JPS5564537A (en) | 1980-05-15 |
JPS599534B2 JPS599534B2 (en) | 1984-03-03 |
Family
ID=15181049
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP53136684A Expired JPS599534B2 (en) | 1978-11-08 | 1978-11-08 | Method for producing bis(3,5-dihydroxymethyl-4-hydroxyphenyl) alkanes |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS599534B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6153929U (en) * | 1984-09-12 | 1986-04-11 | ||
JPH04355502A (en) * | 1991-05-31 | 1992-12-09 | Murata Mfg Co Ltd | Irreversible circuit element |
-
1978
- 1978-11-08 JP JP53136684A patent/JPS599534B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS599534B2 (en) | 1984-03-03 |
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