GB791326A - Improvements in or relating to polyligands containing at least two ª‰-ketomonoacyloxy groups - Google Patents
Improvements in or relating to polyligands containing at least two ª‰-ketomonoacyloxy groupsInfo
- Publication number
- GB791326A GB791326A GB23766/56A GB2376656A GB791326A GB 791326 A GB791326 A GB 791326A GB 23766/56 A GB23766/56 A GB 23766/56A GB 2376656 A GB2376656 A GB 2376656A GB 791326 A GB791326 A GB 791326A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- modified
- phthalate
- castor oil
- glycerol
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Polyligands containing at least two b -ketomono-acyloxy groups are esters of a b -ketomonocarboxylic acid having at least one a -H atom with partial or complete esters of an aliphatic hydroxymonocarboxylic acid and a polyhydric alcohol. Suitable compounds mentioned are the acetoacetates, trichloroacetoacetates, trifluoroacetoacetates, propionoacetates, butyroacetates, caproacetates, a -acetopropionates, g -ethoxyacetoacetates, a -acetophenylacetates, benzoylacetates, 2-furoylacetates, 2-thenoylacetates or a -benzoylpropionates of the partial or complete hydroxyacetates of ethylene glycol, dodecamethylene glycol, or cellulose; the b -hydroxypropionates of propylene glycol or glycerol; the lactates of hexamethylene glycol, or mannitol; the a -hydroxybutyrates of pentaerythritol or sorbitol; the 10-hydroxystearates of erythritol or glycerol; the 9-hydroxystearates of ethylene glycol or glycerol; the glycerate of ethylene glycol; the 9:10-dihydroxystearate of glycerol; or the a -hydroxyvinyl acetate of ethylene glycol. Example X describes the production of the tris-acetoacetate of castor oil and Example XI of the mixed glyceryl ester of acetoacetic acid and of 12-aceto-acetoxyoleic acid. Reference has been directed by the Comptroller to Specification 737,528.ALSO:Polyligands containing at least two b -ketomonoacyloxy groups are esters of a b -ketomonocarboxylic acid having at least one a -H atom with (a) a partial or complete ester of a polyhydric alcohol and an aliphatic hydroxymonocarboxylic acid; or (b) a hydroxy-containing polyhydric alcohol-polycarboxylic acid condensate. Substances (a) above which are mentioned are hydroxy acetates of hydrolysed ethylene/vinyl acetate copolymers or of polyallyl alcohol and lactates of polyvinyl alcohol. Substances (b) above mentioned are condensates of glycerol and phthalic, adipic or tricarballylic acid; sorbitol and sebacic acid; pentaerythritol and succinic acid; ethylene glycol and adipic acid; mannitol and terephthalic acid; polyvinyl alcohol and glutaric acid; polyallyl alcohol and phthalic acid; hydrolysed ethylene/vinyl acetate copolymers and adipic acid. These polyesters may be modified, e.g. with castor oil, coconut oil or with the corresponding acids. b -Keto acids mentioned are: acetoacetic, trichloracetoacetic, trifluoroacetoacetic, propionacetic, butyroacetic, caproacetic, a -acetopropionic, g -ethoxyacetoacetic, a -acetophenylacetic, benzoylacetic, 2-furoylacetic, 2-thenoylacetic and a -benzoylpropionic. In the examples ethyl acetoacetate was heated with: (I) a castor oil modified polyglyceryl phthalate; (II) and (III) a coconut oil modified polyglyceryl phthalate; (IV) a coconut oil acid modified polypentaerythrityl phthalate; (V) a hydrogenated castor oil modified polyglyceryl phthalate. In Example (VI) diketen was used in place of the ethyl acetoacetate of Example (I). In Example (VII) castor oil modified polyglyceryl phthalate was reacted with ethyl trifluoroacetoacetate. Example (VIII) uses coconut oil acid modified polypentaerythrityl phthalate and ethyl trifluoroacetoacetate. In Example (IX) castor oil modified polyglyceryl phthalate was heated with ethyl benzoylacetate. Reference has been directed by the Comptroller to Specification 737,528.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US791326XA | 1953-09-16 | 1953-09-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB791326A true GB791326A (en) | 1958-02-26 |
Family
ID=22148633
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23766/56A Expired GB791326A (en) | 1953-09-16 | 1954-09-01 | Improvements in or relating to polyligands containing at least two ª‰-ketomonoacyloxy groups |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB791326A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0570213A2 (en) * | 1992-05-15 | 1993-11-18 | Scott Bader Company Limited | Terminally modified unsaturated polyester resins |
-
1954
- 1954-09-01 GB GB23766/56A patent/GB791326A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0570213A2 (en) * | 1992-05-15 | 1993-11-18 | Scott Bader Company Limited | Terminally modified unsaturated polyester resins |
EP0570213A3 (en) * | 1992-05-15 | 1994-09-28 | Scott Bader Co | Terminally modified unsaturated polyester resins |
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