JPS55130987A - Production of phosphate diester - Google Patents
Production of phosphate diesterInfo
- Publication number
- JPS55130987A JPS55130987A JP3777179A JP3777179A JPS55130987A JP S55130987 A JPS55130987 A JP S55130987A JP 3777179 A JP3777179 A JP 3777179A JP 3777179 A JP3777179 A JP 3777179A JP S55130987 A JPS55130987 A JP S55130987A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- phosphate
- compound
- hydrolyzed
- production
- 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)
Abstract
PURPOSE: Phosphate triester is hydrolyzed to form title compound by simple operations in a short time in high yield.
CONSTITUTION: A phosphate triester of formula VI (R1 and R2 are organic groups different from each other) is hydrolyzed with water or an alkali such as lithium hydroxide to form a phosphate diester of formula I. The compound of formula VI, the starting material, is obtained by reaction of bis(p-nitrophenyl) phosphate of formula II with a benzoxazolyl ether derivative of formula III in an organic solvent such as benzene to give a compound of formula IV, which is subsequently made to react with an alcohol of R2OH in the presence of CsF. One example of compounds of formula I is 2-methoxyethylphenethyl phosphate and the yield is 80%.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3777179A JPS55130987A (en) | 1979-03-30 | 1979-03-30 | Production of phosphate diester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3777179A JPS55130987A (en) | 1979-03-30 | 1979-03-30 | Production of phosphate diester |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS55130987A true JPS55130987A (en) | 1980-10-11 |
JPS6260387B2 JPS6260387B2 (en) | 1987-12-16 |
Family
ID=12506724
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3777179A Granted JPS55130987A (en) | 1979-03-30 | 1979-03-30 | Production of phosphate diester |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55130987A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110161159A (en) * | 2019-07-04 | 2019-08-23 | 杭州必益泰得医学科技有限公司 | A kind of biological sample analysis method of Oxcarbazepine bioequivalence test |
-
1979
- 1979-03-30 JP JP3777179A patent/JPS55130987A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110161159A (en) * | 2019-07-04 | 2019-08-23 | 杭州必益泰得医学科技有限公司 | A kind of biological sample analysis method of Oxcarbazepine bioequivalence test |
Also Published As
Publication number | Publication date |
---|---|
JPS6260387B2 (en) | 1987-12-16 |
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