JPS5762242A - Preparation of diester-type liquid crystal - Google Patents
Preparation of diester-type liquid crystalInfo
- Publication number
- JPS5762242A JPS5762242A JP55135857A JP13585780A JPS5762242A JP S5762242 A JPS5762242 A JP S5762242A JP 55135857 A JP55135857 A JP 55135857A JP 13585780 A JP13585780 A JP 13585780A JP S5762242 A JPS5762242 A JP S5762242A
- Authority
- JP
- Japan
- Prior art keywords
- group
- liquid crystal
- phenyl
- alkyl
- formula
- 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.)
- Pending
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
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Abstract
PURPOSE: To prepare the titled liquid crystal, in high yield, with simplified process, preventing the formation of impurities by side reactions, by protecting the phenolic hydroxyl group of 4-hydroxybenzoic acid with silyl group, removing the protecting group after esterification, and again esterifying the product.
CONSTITUTION: 4-Hydroxybenzoic acid is reacted with the compound of formula I(R1 and R3 are CH3 or C2H5 and R2 is 4-alkyl-phenyl; or R1 and R2 are 4-alkyl- phenyl and R3 is CH3 or C2H5; or R1WR3 are 4-alkyl-phenyl) to protect the phenolic hydroxyl group, and then subjected to the first-stage esterification reaction. Then the protecting group is removed, and the product is subjected to the second-stage esterification reaction to obtain the objective compound of formula II[R4 and R5 are group of formula IIIWVI (l, m, n, and p are integers 1W10)].
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55135857A JPS5762242A (en) | 1980-10-01 | 1980-10-01 | Preparation of diester-type liquid crystal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55135857A JPS5762242A (en) | 1980-10-01 | 1980-10-01 | Preparation of diester-type liquid crystal |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5762242A true JPS5762242A (en) | 1982-04-15 |
Family
ID=15161389
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP55135857A Pending JPS5762242A (en) | 1980-10-01 | 1980-10-01 | Preparation of diester-type liquid crystal |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5762242A (en) |
-
1980
- 1980-10-01 JP JP55135857A patent/JPS5762242A/en active Pending
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