GB811131A - Improvements in or relating to method of preparing new carboxylic acid and the new carboxylic acid resulting from said method - Google Patents
Improvements in or relating to method of preparing new carboxylic acid and the new carboxylic acid resulting from said methodInfo
- Publication number
- GB811131A GB811131A GB27377/56A GB2737756A GB811131A GB 811131 A GB811131 A GB 811131A GB 27377/56 A GB27377/56 A GB 27377/56A GB 2737756 A GB2737756 A GB 2737756A GB 811131 A GB811131 A GB 811131A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- aliphatic
- ether
- hydroxy
- chloroethyl
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Lubricants (AREA)
Abstract
A polycarboxylic acid is made by condensing an aliphatic coupling agent and a bis-(hydroxy-aryl)-substituted aliphatic acid, said aliphatic coupling agent being an epihalohydrin, an aliphatic dihalide, an aliphatic dihaloether or an aliphatic polyepoxide. Specified coupling agents are 1,2 - dichloroethane, 1,3 - dichloro-propane, 1,4 - dichlorobutane, 1,4 - dichloro-butene, glycol dichlorohydrin, bis-(2-chloro-ethyl) ether, epichlorohydrin, epibromohydrin, 2,3 - epoxypropyl - 2 - hydroxy - 3 - chloropropyl ether, 1,2 - epoxy - 3,4 - epoxybutane and bis-(2,3-epoxypropyl) ether. In the examples, 4,4 - bis - (4 - hydroxy - phenyl) - pentanoic acid is condensed in aqueous caustic soda with: (I) 1,4 - dichlorobutene - 2; (II) 1,4 - dichloro-butane; (III) and (IV) bis-(2-chloroethyl)ether; (V) and (VI) bis-(4-hydroxy-phenyl)-isopropylidene and bis-(2-chloroethyl) ether and (VII) to (X) inclusive epichlorohydrin. The resultant resinous polycarboxylic acids may be esterified with alcoholic hydroxyl groups or epoxide groups and may be used as coatings. The acids may be condensed with polyhydric phenol/epichlorohydrin reaction products and epoxidised vegetable oils. Example (XI) describes the reaction of the product of Example (I) with an epoxidised soya bean oil to form a film. Specifications 768,206 and 790,373 are referred to.ALSO:A polycarboxylic acid is made by condensing an aliphatic coupling agent and a bis (hydroxy aryl) substituted aliphatic acid, said aliphatic coupling agent being an epihalohydrin, an aliphatic dihalide, an aliphatic dihaloether, or an aliphatic poly epoxide. Specified coupling agents are 1,2-dichloro ethane, 1,3-dichloropropane, 1,4 - dichlorobutane, 1,4 - dichlorobutene, glycol dichlorohydrin, bis - (2 - chloroethyl) ether, epichlorohydrin, epibromohydrin, 2,3 - epoxy propyl 2 - hydroxy - 3 - chloropropyl ether, 1,2 - epoxy - 3,4 - epoxybutane, and bis - (2,3 - epoxypropyl) ether. In the examples, 4,4-bis-(4-hydroxy-phenyl) pentanoic acid is condensed in aqueous caustic soda with: (I) 1,4-dichlorobutene-2, (II) 1,4-dichlorobutane, (III) and (IV) bis-(2-chloroethyl) ether, (V) and (VI) bis-(4-hydroxy phenyl) isopropylidene and bis-(2-chloroethyl) ether and (VII) to (X) inclusive epichlorohydrin. Specifications 768,206 and 790,373 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US811131XA | 1955-10-03 | 1955-10-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB811131A true GB811131A (en) | 1959-04-02 |
Family
ID=22162171
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB27377/56A Expired GB811131A (en) | 1955-10-03 | 1956-09-06 | Improvements in or relating to method of preparing new carboxylic acid and the new carboxylic acid resulting from said method |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB811131A (en) |
-
1956
- 1956-09-06 GB GB27377/56A patent/GB811131A/en not_active Expired
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