GB640403A - Improvements in or relating to the production of o-hydroxyphenyl glycerol ether - Google Patents
Improvements in or relating to the production of o-hydroxyphenyl glycerol etherInfo
- Publication number
- GB640403A GB640403A GB981/48A GB98148A GB640403A GB 640403 A GB640403 A GB 640403A GB 981/48 A GB981/48 A GB 981/48A GB 98148 A GB98148 A GB 98148A GB 640403 A GB640403 A GB 640403A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxyphenyl
- relating
- production
- glycidol
- catechol
- 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
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/22—Ethers with hydroxy compounds containing no oxirane rings with monohydroxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
a : b - Dihydroxy - g - (2 - hydroxyphenoxy) - propane is prepared by (1) condensing together equimolecular proportions of catechol and glycidol in the presence of a nitrogen-containing organic base; or (2) condensing catechol monoacetate with glycidol in the presence of pyridine and hydrolysing the resulting a : b -dihydroxy-g -(2-acetoxyphenoxy)-propane. In either case, the reaction is initiated by warming, and the temperature is prevented from rising above about 110 DEG C. by external cooling. In method (1), the organic base may be pyridine, picoline, quinoline, dimethylaniline, a primary amine (e.g. ethylamine) or a secondary amine (e.g. dimethylamine). In method (2), the hydrolysis may be effected by alkali, e.g. potassium hydroxide in ethyl alcohol. An example is given of each method. Specification 628,497 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB981/48A GB640403A (en) | 1948-01-13 | 1948-01-13 | Improvements in or relating to the production of o-hydroxyphenyl glycerol ether |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB981/48A GB640403A (en) | 1948-01-13 | 1948-01-13 | Improvements in or relating to the production of o-hydroxyphenyl glycerol ether |
Publications (1)
Publication Number | Publication Date |
---|---|
GB640403A true GB640403A (en) | 1950-07-19 |
Family
ID=9713920
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB981/48A Expired GB640403A (en) | 1948-01-13 | 1948-01-13 | Improvements in or relating to the production of o-hydroxyphenyl glycerol ether |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB640403A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1150092B (en) * | 1958-04-24 | 1963-06-12 | Bayer Ag | Process for the production of monoglycol and chlorohydric binary ethers |
-
1948
- 1948-01-13 GB GB981/48A patent/GB640403A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1150092B (en) * | 1958-04-24 | 1963-06-12 | Bayer Ag | Process for the production of monoglycol and chlorohydric binary ethers |
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