GB675665A - Improvements in and relating to the production of polymeric compounds - Google Patents
Improvements in and relating to the production of polymeric compoundsInfo
- Publication number
- GB675665A GB675665A GB570549A GB570549A GB675665A GB 675665 A GB675665 A GB 675665A GB 570549 A GB570549 A GB 570549A GB 570549 A GB570549 A GB 570549A GB 675665 A GB675665 A GB 675665A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mol
- epichlorhydrin
- aniline
- refluxed
- alcohol
- 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
- C08G65/04—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
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
- C08G73/0213—Preparatory process
- C08G73/022—Preparatory process from polyamines and epihalohydrins
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Compounds (AREA)
Abstract
Polymeric compounds, capable of being drawn into fibres, are produced by reacting in substantially equimolecular proportions epichlorhydrin and an amine of formula R.NH2, where R is an aryl or aralkyl group containing only carbon and hydrogen, together with alkali in an amount at least equivalent to the chlorine content of the epichlorhydrin. Specified amines are aniline, benzylamine and paratoluidine or mixtures thereof. The amine may be replaced in part by a carboxyl substituted primary amine (e.g. para-amino benzoic acid) or by a dihydric phenol in which the carbon atoms linked to the hydroxyl groups are separated by at least one other carbon atom (e.g. hydroquinone). The reaction may be performed (a) by heating the amine, epichlorhydrin and alkali together; (b) by reacting epichlorhydrin and the amine to form a compound R.NH.CH(OH).CH2Cl which is heated with alkali to form a compound <FORM:0675665/IV (a)/1> which may or may not be isolated prior to heating it to polymerize it; (c) by reacting epichlorhydrin, the dihydric phenol and alkali to form a bisglycidyl ether which is then heated with the amine. In examples: (1) aniline (1 mol.) and epichlorhydrin (1 mol.) are heated together and the product is dissolved in alcohol and refluxed with caustic soda (1.15 mol.); (2) aniline (1 mol.), epichlorhydrin (1 mol.) and sodium carbonate (0.56 mol.) are refluxed in presence of water and alcohol. The product is dissolved in dilute hydrochloric acid and precipitated with aqueous caustic soda solution; (3) aniline (1 mol.) and epichlorhydrin (1 mol.) are allowed to stand at room temperature and the product refluxed with sodium bicarbonate (1.1 mol.) in presence of water and alcohol; (4) aniline (1 mol.), epichlorhydrin (1 mol.), water and alcohol are refluxed, caustic soda (1.1 mol.) added and the mixture refluxed; (5) benzylamine (1 mol.), epichlorhydrin (1 mol.) and alcohol are mixed, sodium carbonate (0.56 mol.) added and the mixture refluxed; (6) aniline (1 mol.), epichlorhydrin (1.1 mol.), and alcohol are refluxed, sufficient alcoholic potash added to precipitate all the potassium chloride, the alcohol and excess epichlorhydrin removed by distillation, the residue distilled at 2 mm. of mercury and the distillate heated to yield a polymer soluble in hot dilute aqueous mineral acid; (7) aniline (1 mol.), epichlorhydrin (1 mol.), sodium bicarbonate (1.1 mol.) and water are refluxed; (8) aniline (1 mol.), hydroquinone bis-glycidyl ether (1 mol.) alcohol, and aqueous caustic soda solution are refluxed. Specifications 438,523, 628,821, 652,024 and 652,030 are referred to.ALSO:Compounds of formula <FORM:0675665/IV (b)/1> where R is an aryl or aralkyl hydrocarbon group, are produced by reacting a primary amine of formula R.NH2 with epichlorhydrin. Specified primary amines are aniline, benzylamine and paratoluidine. The compounds of formula NHR.CH2.CH(OH).CH2Cl react with alkalies to give compounds of formula <FORM:0675665/IV (b)/2> The latter compounds polymerize on heating (see Group IV (a)). Specification 438,523 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB570549A GB675665A (en) | 1949-03-02 | 1949-03-02 | Improvements in and relating to the production of polymeric compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB570549A GB675665A (en) | 1949-03-02 | 1949-03-02 | Improvements in and relating to the production of polymeric compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB675665A true GB675665A (en) | 1952-07-16 |
Family
ID=9801090
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB570549A Expired GB675665A (en) | 1949-03-02 | 1949-03-02 | Improvements in and relating to the production of polymeric compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB675665A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2753372A (en) * | 1953-11-19 | 1956-07-03 | American Cyanamid Co | Water-dispersible aliphatic amine-epichlorohydrin reaction products |
DE961490C (en) * | 1951-10-05 | 1957-04-04 | Rohm & Haas | Process for the production of weakly basic anion exchange resins |
US3240720A (en) * | 1960-04-22 | 1966-03-15 | Minnesota Mining & Mfg | Bifunctional monomers and process for their production |
US3257249A (en) * | 1963-06-06 | 1966-06-21 | Thiokol Chemical Corp | Method of making acetylenic epoxy amino compounds |
US3257250A (en) * | 1963-06-06 | 1966-06-21 | Thiokol Chemical Corp | Acetylenic epoxy amino compounds and method of making the same |
DE1238214B (en) * | 1960-02-22 | 1967-04-06 | Montedison Spa | Process for the production of nitrogen-containing condensation products |
-
1949
- 1949-03-02 GB GB570549A patent/GB675665A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE961490C (en) * | 1951-10-05 | 1957-04-04 | Rohm & Haas | Process for the production of weakly basic anion exchange resins |
US2753372A (en) * | 1953-11-19 | 1956-07-03 | American Cyanamid Co | Water-dispersible aliphatic amine-epichlorohydrin reaction products |
DE1238214B (en) * | 1960-02-22 | 1967-04-06 | Montedison Spa | Process for the production of nitrogen-containing condensation products |
US3240720A (en) * | 1960-04-22 | 1966-03-15 | Minnesota Mining & Mfg | Bifunctional monomers and process for their production |
US3257249A (en) * | 1963-06-06 | 1966-06-21 | Thiokol Chemical Corp | Method of making acetylenic epoxy amino compounds |
US3257250A (en) * | 1963-06-06 | 1966-06-21 | Thiokol Chemical Corp | Acetylenic epoxy amino compounds and method of making the same |
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