GB693980A - Process for preparing linear polyethers - Google Patents
Process for preparing linear polyethersInfo
- Publication number
- GB693980A GB693980A GB1950650A GB1950650A GB693980A GB 693980 A GB693980 A GB 693980A GB 1950650 A GB1950650 A GB 1950650A GB 1950650 A GB1950650 A GB 1950650A GB 693980 A GB693980 A GB 693980A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diol
- disulphonic
- ester
- specified
- molecular proportion
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
- C08G65/4093—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group characterised by the process or apparatus used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols
- C08G65/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives derived from phenols from phenols (I) and other compounds (II), e.g. OH-Ar-OH + X-Ar-X, where X is halogen atom, i.e. leaving group
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
Abstract
Linear polyethers having a recurrent unit [Ar-O-R-O], where Ar is an arylene group and R is a divalent linkage group, are made by reacting substantially equimolecular proportions of a dihydric phenol and a disulphonic ester of a diol in presence of an alkali the molecular proportion of which is at least twice the molecular proportion of the disulphonic ester. Specified dihydric phenols are resorcinol, hydroquinone and 3,31- or 4, 41-dihydroxydiphenyl. Specified disulphonic esters are the di-paratoluene sulphonates of ethylene glycol; 1 : 4-bis - (beta - hydroxyethoxy) - benzene; propane - 1,3 - diol; butane - 1,4 - diol; pentane-1,5 - diol; hexane - 1,6 - diol; decane - 1,10-diol; and diethylene glycol. Reaction may be performed in presence of a mixture of dioxane and water. The polymers may be purified by washing with boiling water and boiling hydrochloric acid. They are soluble in meta-cresol and nitrobenzene. Examples are given. Specification 433,452 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1950650A GB693980A (en) | 1950-08-04 | 1950-08-04 | Process for preparing linear polyethers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1950650A GB693980A (en) | 1950-08-04 | 1950-08-04 | Process for preparing linear polyethers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB693980A true GB693980A (en) | 1953-07-08 |
Family
ID=10130496
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1950650A Expired GB693980A (en) | 1950-08-04 | 1950-08-04 | Process for preparing linear polyethers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB693980A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1259333B (en) * | 1964-03-09 | 1968-01-25 | Minnesota Mining & Mfg | Process for the preparation of N-alkyl-perfluoroalkanesulphone-amidoalkyl-arylsulphonic acid esters |
-
1950
- 1950-08-04 GB GB1950650A patent/GB693980A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1259333B (en) * | 1964-03-09 | 1968-01-25 | Minnesota Mining & Mfg | Process for the preparation of N-alkyl-perfluoroalkanesulphone-amidoalkyl-arylsulphonic acid esters |
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