GB864097A - Polyether derivatives - Google Patents
Polyether derivativesInfo
- Publication number
- GB864097A GB864097A GB618958A GB618958A GB864097A GB 864097 A GB864097 A GB 864097A GB 618958 A GB618958 A GB 618958A GB 618958 A GB618958 A GB 618958A GB 864097 A GB864097 A GB 864097A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkylene oxides
- polyepoxides
- polyethers
- melt
- specified
- 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
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
- C07H15/08—Polyoxyalkylene derivatives
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4895—Polyethers prepared from polyepoxy compounds
-
- 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
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Polyethers (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Polyethers are prepared by reacting polyhydroxy compounds with alkylene oxides alone or together with polyepoxides, using dimethyl sulphoxide as reaction medium. The polyhydroxy compounds must melt at temperatures above 120 DEG C. or melt only with decomposition and must be soluble in dimethyl sulphoxide. Suitable compounds are trimethylolethane, pentaerythritol, tetramethylolcyclohexanol, sucrose, a -methyl glucoside and other sugars, mannitol, inositol and quebrachitol. Specified alkylene oxides are ethylene, propylene and butylene oxides. Specified polyepoxides are 1:2-3:4-diepoxybutane, diallyl ether dioxide and 2,6-dioxaspiro-[3,3]-heptane. The reaction may be effected at temperatures of 50 DEG to 150 DEG C. and in the presence of alkaline catalyst. Examples are given in which the reactions are carried out under nitrogen, the catalyst neutralised with adipic acid and then the polyethers bleached with hydrogen peroxide. According to the Provisional Specification, epihalo hydrins such as epichlorhydrin, may be used in place of or in admixture with the alkylene oxides.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB618958A GB864097A (en) | 1958-02-26 | 1958-02-26 | Polyether derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB618958A GB864097A (en) | 1958-02-26 | 1958-02-26 | Polyether derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
GB864097A true GB864097A (en) | 1961-03-29 |
Family
ID=9810045
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB618958A Expired GB864097A (en) | 1958-02-26 | 1958-02-26 | Polyether derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB864097A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1245385B (en) * | 1962-08-28 | 1967-07-27 | Olin Mathieson | Process for the preparation of oxyalkylation products of di- or triamino-1, 3, 5-triazines |
FR2489344A1 (en) * | 1980-09-02 | 1982-03-05 | Texaco Development Corp | PROCESS FOR PREPARING HIGH VISCOSITY FLUIDS |
FR2489341A1 (en) * | 1980-09-02 | 1982-03-05 | Texaco Development Corp | POLYOLS MODIFIED BY EPOXY RESINS, PROCESS FOR THEIR PREPARATION AND USE THEREOF FOR THE PREPARATION OF POLYURETHANE FOAMS |
EP1403289A1 (en) * | 2001-05-14 | 2004-03-31 | Kuraray Co., Ltd. | MODIFIED ETHYLENE−VINYL ALCOHOL COPOLYMER AND METHOD FOR THE PRODUCTION THEREOF |
-
1958
- 1958-02-26 GB GB618958A patent/GB864097A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1245385B (en) * | 1962-08-28 | 1967-07-27 | Olin Mathieson | Process for the preparation of oxyalkylation products of di- or triamino-1, 3, 5-triazines |
FR2489344A1 (en) * | 1980-09-02 | 1982-03-05 | Texaco Development Corp | PROCESS FOR PREPARING HIGH VISCOSITY FLUIDS |
FR2489341A1 (en) * | 1980-09-02 | 1982-03-05 | Texaco Development Corp | POLYOLS MODIFIED BY EPOXY RESINS, PROCESS FOR THEIR PREPARATION AND USE THEREOF FOR THE PREPARATION OF POLYURETHANE FOAMS |
EP1403289A1 (en) * | 2001-05-14 | 2004-03-31 | Kuraray Co., Ltd. | MODIFIED ETHYLENE−VINYL ALCOHOL COPOLYMER AND METHOD FOR THE PRODUCTION THEREOF |
EP1403289A4 (en) * | 2001-05-14 | 2004-12-22 | Kuraray Co | Modified ethylene-vinyl alcohol copolymer and method for the production thereof |
US7811646B2 (en) | 2001-05-14 | 2010-10-12 | Kuraray Co., Ltd. | Modified ethylene-vinyl alcohol copolymer and method for the production thereof |
US8329818B2 (en) | 2001-05-14 | 2012-12-11 | Kuraray Co., Ltd. | Modified ethylene-vinyl alcohol copolymer and method for the production thereof |
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