GB918360A - Bis-1,3-dioxolanes - Google Patents
Bis-1,3-dioxolanesInfo
- Publication number
- GB918360A GB918360A GB3267961A GB3267961A GB918360A GB 918360 A GB918360 A GB 918360A GB 3267961 A GB3267961 A GB 3267961A GB 3267961 A GB3267961 A GB 3267961A GB 918360 A GB918360 A GB 918360A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bis
- iii
- carbon atoms
- divinyl
- formula
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F24/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/156—Heterocyclic compounds having oxygen in the ring having two oxygen atoms in the ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Paints Or Removers (AREA)
Abstract
Bis-1,3-dioxolanes having the formula <PICT:0918360/III/1> in which R is a tetravalent organic radical having at least 2 carbon atoms, each terminal carbon atom of the radical being a member of one dioxolane ring, and X is an organic radical comprising 2 carbon atoms in the dioxolane ring, at least one of said carbon atoms in X bearing an alkenyl substituent, are used for the production of coating compositions which can be applied and dried at room temperature or for a short time at slightly elevated temperature, e.g. 50 DEG -150 DEG C., to give hard, glossy films. The compounds are usually mixed with metallic driers such as lead, manganese, zinc, iron, nickel, cadmium, copper, tin, zirconium and, preferably, cobalt salts. Suitable salts, for example, are acetates, naphthenates, linoleates, resinates, tallates, oxalates and phthalates. Other additives which may be used as solvents, plasticizers, pigments, extenders, inhibitors and flow-control agents. Other film-forming materials, such as polymers and copolymers of acrylic esters, vinyl acetate and styrene and unsaturated polyesters may also be added to the compositions. Examples are given of the preparation of coating compositions by mixing (a) the compound of formula <PICT:0918360/III/2> with (i) cobalt butyl phthalate solution to give a clear hard film at room temperature in a few days and at 110 DEG C. in 20 mins. and (ii) with titanium dioxide, toluene and cobalt butyl phthalate to give a coating composition which could be sprayed on glass ceramics, wood and metal; (b) a compound of the general formula given above, in which R is <FORM:0918360/III/1> and X is <FORM:0918360/III/2> is mixed with 1% of cobalt butyl phthalate to give a film drying at room temperature in a few days and at 110 DEG C. in 30 mins.; (c) a compound of the general formula given above in which R is <FORM:0918360/III/3> and X is <FORM:0918360/III/4> is mixed with a small amount of cobalt butyl phthalate to give a composition which is used for coating steel panels; (d) bis-(4,5-divinyl-1,3-dioxol-2-yl) benzene is mixed with toluene and cobalt butyl phthalate to give a coating composition for steel panels; and (e) the compound of formula <FORM:0918360/III/5> is mixed with 1% of cobalt butyl phthalate and used as a coating composition for panels.ALSO:The invention comprises bis-1,3-dioxolanes of the formula <FORM:0918360/IV (b)/1> in which R is a tetravalent organic radical having at least 2 carbon atoms, each terminal carbon atom of the radical being a member of one dioxolane ring, and X is an organic radical comprising 2 carbon atoms in the dioxolane ring, at least one of said ring carbon atoms carrying an alkenyl substituent. Preferably the terminal carbon atoms in R carry a hydrogen atom. The compounds may be prepared by reacting at least one alkenyl substituted ethylene glycol of formula HO-X-OH with at least one dialdehyde or diketone of formula O=R=O, or lower alkyl tetraacetals or ketals thereof, at a temperature of 50-150 DEG C. in the presence of an acidic catalyst. Suitable alkenyl substituted glycols are, for example, 1,2-divinyl; 1,2-diisopropenyl-; 1,2-di-(a -isopropylvinyl)-; 1,2 - dipropenyl-; 1,2 - divinyl - 1,2-dimethyl-; 1,2 - dibut - 11 - enyl-; 1,2-dipent-11-enyl-; 1,2-di-(hepta-1,3,5-trienyl)-; 1,2-dihex-11-enyl-; 1,2-dihept-11-enyl-; 1,2-diphenyl-1,2-divinyl-; 1,2 - dithenyl - 1,2 - divinyl-; 1-vinyl-2-thenyl-; 1,2-di-(2-methylpropen-1-yl)-; 1-vinyl-; 1-vinyl-2-cyclohexyl-; 1-isopropenyl-; 1-furyl-2 - vinyl-; and 1,1-divinyl-2-furfuryl-ethylene glycol. Suitable aldehydes, ketones, acetals and ketals are glyoxal; glutaraldehyde; adipaldehyde; terephthaldehyde; 2,5-furan-diol; oxybis-(5-methylene-2-furfuraldehyde); 2,5-furandi-(3-propional); 1,2-di-(6-formyl-2-tetrahydro-pyranoxy)ethane; 2,2-bis[p-6-formyl - 2 - tetrahydropyranoxy)-phenyl]propane; dodecane-1, 12-diol; 1,1,3,3-tetraethoxy propane; 1,1,3-trimethoxy-3-ethoxy propane; suberic dialdehyde tetraethyl acetal; 1,1,4,4-tetraethoxy ethane; 1,1,7,7-tetraethoxy-hept-3,4-ene; 2,2,5,5-tetraethoxyfuran; cyclohexane - 1,6 - dione; acetonyl acetone; 1,3-diphenyl-1,3-propane-dione; 1,4-dimethyl-1,1,4,4-tetraethoxy butane and 1,8-diethyl-1,1,8,8-tetramethoxy octane. Suitable catalysts are, for example, strong mineral acids, which may be deposited on silica-alumina carriers, or organic acids. Stablizers, e.g. hydroquinone or tertiary butyl catechol, may be added to the reaction mixture. Examples are given of the preparation of various of the new compounds and it is stated that bis-[4-(a -chlorovinyl)-5-vinyl-1,3-dioxol-2-yl]methane may be prepared in a similar manner. 2,2 - Bis - [p-(6-formyl-2-tetrahydropyranoxy) phenyl]-propane used as starting material in Example 5 is prepared by reacting 2,2-bis-(41-hydroxyphenyl)propane with bisacrolein.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US5738960A | 1960-09-21 | 1960-09-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB918360A true GB918360A (en) | 1963-02-13 |
Family
ID=22010284
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3267961A Expired GB918360A (en) | 1960-09-21 | 1961-09-12 | Bis-1,3-dioxolanes |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE608042A (en) |
GB (1) | GB918360A (en) |
NL (1) | NL269459A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102408332A (en) * | 2011-11-14 | 2012-04-11 | 无锡英普林纳米科技有限公司 | Ultraviolet curing degradable cross-linking monomer and preparation method thereof |
-
1961
- 1961-09-11 BE BE608042A patent/BE608042A/fr unknown
- 1961-09-12 GB GB3267961A patent/GB918360A/en not_active Expired
- 1961-09-21 NL NL269459D patent/NL269459A/nl unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102408332A (en) * | 2011-11-14 | 2012-04-11 | 无锡英普林纳米科技有限公司 | Ultraviolet curing degradable cross-linking monomer and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
BE608042A (en) | 1962-03-11 |
NL269459A (en) | 1964-06-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2437648A (en) | Catalytic oxidation of unsaturated organic compounds | |
Reddi et al. | N-Heterocyclic carbene catalyzed regioselective oxo-acyloxylation of alkenes with aromatic aldehydes: a high yield synthesis of α-acyloxy ketones and esters | |
US2399214A (en) | Convertible alkyd resins | |
GB918360A (en) | Bis-1,3-dioxolanes | |
Frimer et al. | Superoxide anion radical (O2. bul.-)-mediated base-catalyzed autoxidation of enones | |
JPH0532390B2 (en) | ||
Kharasch et al. | Reactions of atoms and free radicals in solution. XXXI. Reations of free benzoyl radicals with azo compounds | |
US3196118A (en) | Coating compositions containing an amine and a metallic drier | |
US3441423A (en) | Coating compositions containing polyunsaturated bis-1,3-dioxolanes | |
US3245927A (en) | Coating compositions containing cyclic acetals | |
Kang et al. | Stereospecific stille-coupling reaction of (Z)-1, 2-bis (trimethylstannyll) ethenes with hypervalent iodonium salts | |
US3320195A (en) | Coating compositions containing a tetrasubstituted guanidine | |
US2864852A (en) | Acylated keto esters and keto nitriles | |
GB644597A (en) | Mixed esters | |
US2894849A (en) | Alpha, gamma diketones in combination with metallo-organic driers as drying accelerators for siccative coatings | |
US3184441A (en) | Air-drying esters of 1, 3-cyclic acetals | |
GB959320A (en) | A method for polymerizing aldehydes | |
JP4800927B2 (en) | Method for producing lactone or epoxide | |
US3058934A (en) | Coating compositions containing z-vinyl- | |
US2957035A (en) | Copolymerizable methylene-substituted cycloalkenes, their preparation, coating compositions containing them and polymers thereof | |
GB802022A (en) | Dioxolanes | |
US2604489A (en) | Ether esters of glycerol | |
US2540053A (en) | Halogen substituted gamma, gammadicarbalkoxybutyraldehydes and process | |
US3413352A (en) | Preparation of substituted aldehydes and ketones from vinyl esters | |
US3600384A (en) | Reaction of 1,2-bis(3-cyclohexen-1-yl) ethylenes with certain unsaturated compounds and product obtained thereby |