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US4296005A
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Adducts containing hydroxyl groups from mononuclear hydantoin glycidyl compounds and non-aromatic dicarboxylic acids
Assignee: BASF Corp
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Filing: 1980-10-27
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Granted: 1981-10-20
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Expires: 2000-10-27
Abstract
Abstract An advanced addition product containing hydroxyl groups is prepared from the reaction of specific mononuclear hydantoin glycidyl compounds with non-aromatic dicarboxylic acids of 9 to 44 carbon atoms and, optionally mono-carboxylic acids of 6 to 18 carbon atoms. The above advanced addition products are heat curable with suitable curing agents for hydroxyl containing materials to afford cured compositions exhibiting excellent weathering, color stability and chalking resistance.
Inventors
- 👤 Marianne Di Benedetto
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-25 08:11
CPC Classifications
C; C08; C08L; C08L63/00; C08G; C08G59/00; C08G59/18; C08G59/20; C08G59/22; C08G59/26; C08G59/40; C08G59/42; C08G59/4292
Claims Analysis
Total Claims: 15
Claim 1
Independent Claim
168 words
An advanced addition product containing hydroxyl groups, which is obtained by heating a mixture comprising: (a) one equivalent of a mononuclear hydantoin glycidyl compound selected from the group consisting of (1) a compound of the formula I ##STR8## (2) a compound of the formula II ##STR9## (3) a compound of the formula III ##STR10## (4) any combination of compounds of the formulae I, II, or III, wherein R 1 , R 2 , R 3 , R 4 , R 6 and R 7 are independently alkyl of 1 to 8 carbon atoms or cycloalkyl of 5 to 6 carbon atoms or R 1 and R 2 together, R 3 and R 4 together and R 6 and R 7 together are tetramethylene or pentamethylene, and R 5 and R 8 independently are hydrogen or methyl; (b) 0.7 to 2.0 equivalents of a non-aromatic dicarboxylic acid of 9 to 44 carbon atoms; and (c) 0.0 to 0.5 equivalents of a monocarboxylic acid of 6 to 18 carbon atoms.
Claim 2
Dependent Claim
168 words
An advanced addition product containing hydroxyl groups, which is obtained by heating a mixture comprising: (a) one equivalent of a mononuclear hydantoin glycidyl compound selected from the group consisting of (1) a compound of the formula I ##STR8## (2) a compound of the formula II ##STR9## (3) a compound of the formula III ##STR10## (4) any combination of compounds of the formulae I, II, or III, wherein R 1 , R 2 , R 3 , R 4 , R 6 and R 7 are independently alkyl of 1 to 8 carbon atoms or cycloalkyl of 5 to 6 carbon atoms or R 1 and R 2 together, R 3 and R 4 together and R 6 and R 7 together are tetramethylene or pentamethylene, and R 5 and R 8 independently are hydrogen or methyl; (b) 0.7 to 2.0 equivalents of a non-aromatic dicarboxylic acid of 9 to 44 carbon atoms; and (c) 0.0 to 0.5 equivalents of a monocarboxylic acid of 6 to 18 carbon atoms.
Claim 3
Dependent Claim
35 words
An advanced addition product according to claim 1 wherein R 1 , R 2 , R 3 , R 4 , R 6 and R 7 are independently alkyl to 1 to 8 carbon atoms.
Claim 4
Dependent Claim
29 words
An advanced addition product according to claim 1 wherein the mononuclear hydantoin glycidyl compound is selected from the group consisting of 1,3-diglycidyl-5,5-dimethylhydantoin; 1,3-diglycidyl-5-ethyl-5-methylhydantoin; 1,3-diglycidyl-5-sec-amyl-5-ethylhydantoin; 1-glycidyl-3-(glycidyloxy-2'-propyl)-5,5-dimethylhydantoin; 1-glycidyl-3-(2'-hydroxypropyl)-5,5-dimethylhydantoin; and mixtures thereof.
Claim 5
Dependent Claim
19 words
An advanced addition product according to claim 1, wherein the non-aromatic dicarboxylic acid contains 17 to 36 carbon atoms.
Claim 6
Dependent Claim
35 words
An advanced addition product according to claim 1, wherein the non-aromatic dicarboxylic acid is selected from the group consisting of aliphatic dicarboxylic acids, dibasic fatty acids and a dicarboxylic acid of the formula VI ##STR11##
Claim 7
Dependent Claim
29 words
An advanced addition product, according to claim 1, prepared by heating a mixture of (a) 1,3-diglycidyl-5-sec-amyl-5-ethylhydantoin, 1-glycidyl-3-(glycidyloxy-2'-propyl)-5,5-dimethylhydantoin, and 1-glycidyl-3-(2'-hydroxypropyl)-5,5-dimethylhydantoin and (b) a dicarboxylic acid of the formula VI ##STR12##
Claim 8
Dependent Claim
26 words
An advanced addition product, according to claim 1, prepared by heating a mixture of (a) 1,3-diglycidyl-5-ethyl-5-methylhydantoin and (b) a dicarboxylic acid of the formula VI ##STR13##
Claim 9
Dependent Claim
28 words
An advanced addition product, according to claim 1, prepared by heating a mixture of (a) 1-glycidyl-3-(glycidyloxy-2'-propyl)-5,5-dimethylhydantoin and 1-glycidyl-3-(-2'-hydroxypropyl)5,5-dimethylhydantoin and (b) a dicarboxylic acid of the formula VI ##STR14##
Claim 10
Dependent Claim
29 words
An advanced addition product, according to claim 1, prepared by heating a mixture of (a) 1,3-diglycidyl-5,5-dimethylhydantoin, 1-glycidyl-3-(glycidyloxy-2'-propyl)-5,5-dimethylhydantoin and 1-glycidyl-3-(2'-hydroxypropyl)-5,5-dimethylhydantoin and (b) a dicarboxylic acid of the formula VI ##STR15##
Claim 11
Dependent Claim
29 words
An advanced addition product, according to claim 1, prepared by heating a mixture of (a) 1,3-diglycidyl-5-sec-amyl-5-ethylhydantoin, 1-glycidyl-3-(glycidyloxy-2'-propyl)-5,5-dimethylhydantoin and 1-glycidyl-3-(2'-hydroxypropyl)-5,5-dimethylhydantoin and (b) a dibasic fatty acid of 36 carbon atoms.
Claim 12
Dependent Claim
36 words
An advanced addition product, according to claim 1, prepared by heating a mixture consisting essentially of (a) one equivalent of the mononuclear hydantoin glycidyl compound; and (b) 0.8 to 1.2 equivalents of the non-aromatic dicarboxylic acid.
Claim 13
Dependent Claim
22 words
A heat curable composition which comprises an advanced addition product containing hydroxyl groups according to claim 1 and a curing agent therefor.
Claim 14
Dependent Claim
15 words
A heat curable composition according to claim 12, wherein the curing agent is an aminoplast.
Claim 15
Dependent Claim
19 words
A heat curable composition according to claim 13 wherein the aminoplast is a melamine-formaldehyde resin or an urea-formaldehyde resin.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1984-10-19 | 1985-04-20 | 1985-10-20 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1988-10-19 | 1989-04-20 | 1989-10-20 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1992-10-19 | 1993-04-20 | 1993-10-20 | $7700.00 | Window Closed / Lapsed |