GB1047557A - Polymers of epoxy-halo-substituted alkanes - Google Patents
Polymers of epoxy-halo-substituted alkanesInfo
- Publication number
- GB1047557A GB1047557A GB1869765A GB1869765A GB1047557A GB 1047557 A GB1047557 A GB 1047557A GB 1869765 A GB1869765 A GB 1869765A GB 1869765 A GB1869765 A GB 1869765A GB 1047557 A GB1047557 A GB 1047557A
- Authority
- GB
- United Kingdom
- Prior art keywords
- halo
- epoxy
- glycol
- alkane
- water
- 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
- C08G65/02—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
- C08G65/2642—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 characterised by the catalyst used
- C08G65/2645—Metals or compounds thereof, e.g. salts
- C08G65/2654—Aluminium or boron; Compounds thereof
-
- 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
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5003—Polyethers having heteroatoms other than oxygen having halogens
- C08G18/5006—Polyethers having heteroatoms other than oxygen having halogens having chlorine and/or bromine atoms
-
- 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
- C08G65/04—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 only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
- C08G65/24—Epihalohydrins
Abstract
Epoxy-halo-substituted alkanes containing a vic-epoxy group at least one carbon atom of which is directly attached to a halogen-bearing carbon atom, are polymerized firstly by contacting said compound with water or an organic dihydroxy compound in the presence of boron trifluoride at a temperature from 60-90 DEG C. to give an adduct in which the mole ratio of the epoxy-halo-substituted alkane to the water or dihydroxy compound is not less than 2: 1 and not greater than 6: 1, and then reacting said adduct with further epoxy-halo-substituted alkane at a temperature from -30 DEG to 40 DEG C. to give a polymer in which the mole ratio of the epoxy-halo-substituted alkane to the water or dihydroxy compound is not less than 4: 1. The reaction may be carried out in an organic nonhydroxylic solvent, preferably a polyhalosubstituted alkane such as methylene dichloride, ethylene dichloride and chloroform; dioxan may be used. The preferred epoxy-halo-substituted alkane is epichlorhydrin but others including epibromhydrin, 2 - methylepichlorhydrin, 2-ethylepibromhydrin, 1,4 - dichloro - 2,3 - epoxybutane and 1 - chloro - 2,3 - epoxypentane, may be used. Water is the preferred initiator but monoethylene glycol, diethylene glycol, triethylene glycol, monopropylene glycol, dipropylene glycol, tripropylene glycol, resorcinol and orcinol are among suitable organic dihydroxy compounds. Molecular weights of 2000-2500 are obtained by using controlled quantities of the halo-alkane solvent.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1869765A GB1047557A (en) | 1965-05-04 | 1965-05-04 | Polymers of epoxy-halo-substituted alkanes |
FR59880A FR1478151A (en) | 1965-05-04 | 1966-05-02 | Process for the preparation of epoxy-halo-alkane polymers |
NL6605888A NL6605888A (en) | 1965-05-04 | 1966-05-02 | |
BE680431D BE680431A (en) | 1965-05-04 | 1966-05-03 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1869765A GB1047557A (en) | 1965-05-04 | 1965-05-04 | Polymers of epoxy-halo-substituted alkanes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1047557A true GB1047557A (en) | 1966-11-09 |
Family
ID=10116857
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1869765A Expired GB1047557A (en) | 1965-05-04 | 1965-05-04 | Polymers of epoxy-halo-substituted alkanes |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE680431A (en) |
GB (1) | GB1047557A (en) |
NL (1) | NL6605888A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2426060A1 (en) * | 1978-05-17 | 1979-12-14 | Minnesota Mining & Mfg | COLORLESS HYDROXY TERMINATED POLY (CHLOROALKYLEN ETHERS) |
FR2465760A2 (en) * | 1979-09-18 | 1981-03-27 | Minnesota Mining & Mfg | HALOGENOALKYLENE POLY (ETHERS) WITH HYDROXY TERMINATION AND CATALYTIC SYSTEM FOR THEIR PREPARATION |
EP0094014A1 (en) * | 1982-05-06 | 1983-11-16 | The B.F. GOODRICH Company | Process for preparing colorless hydroxyl epihalohydrin polymers |
-
1965
- 1965-05-04 GB GB1869765A patent/GB1047557A/en not_active Expired
-
1966
- 1966-05-02 NL NL6605888A patent/NL6605888A/xx unknown
- 1966-05-03 BE BE680431D patent/BE680431A/xx unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2426060A1 (en) * | 1978-05-17 | 1979-12-14 | Minnesota Mining & Mfg | COLORLESS HYDROXY TERMINATED POLY (CHLOROALKYLEN ETHERS) |
FR2465760A2 (en) * | 1979-09-18 | 1981-03-27 | Minnesota Mining & Mfg | HALOGENOALKYLENE POLY (ETHERS) WITH HYDROXY TERMINATION AND CATALYTIC SYSTEM FOR THEIR PREPARATION |
EP0094014A1 (en) * | 1982-05-06 | 1983-11-16 | The B.F. GOODRICH Company | Process for preparing colorless hydroxyl epihalohydrin polymers |
Also Published As
Publication number | Publication date |
---|---|
BE680431A (en) | 1966-11-03 |
NL6605888A (en) | 1966-11-07 |
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