Patent US4568123A successfully refreshed from Google Patents.
Patent US4751254A successfully refreshed from Google Patents.
US4751254A
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US
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Process for in situ coloration of thermosetting resins
Assignee: MILLIKEN RESEARCH Corp SPARTANBURG COUNTY OF SPARTANBURG SOUTH CAROLINA A CORP OF
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Filing: 1987-01-20
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Granted: 1988-06-14
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Expires: 2007-01-20
Abstract
Abstract This invention relates to a process for coloring polyurethane resins during the production of same with reactive colorants derived from novel polyalkoxytrifluoroaniline intermediates. These colorants impart increased brightness in shade for both aromatic and heteroaromatic derivatives and increased resistance to stannous octanoate catalyst over conventional polymeric colorants derived for heteroaromatic compounds. These novel colorants have the structure: ##STR1## wherein R 1 is selected from H, a lower alkyl group containing from 1 to about 10 carbon atoms, CH 2 Cl, CH 2 OH, phenyl or ##STR2## where R 6 is H or a lower alkyl group containing from 1 to about 9 carbon atoms; R 2 is selected from OH, NH 2 or SH; R 3 is selected from a lower alkyl group containing from 1 to about 9 carbon atoms, cyanoalkyl, acetoxyalkyl or ##STR3## where R 1 and R 2 are as given above; R 4 is H, CF 3 , a lower alkyl group containing from 1 to about 9 carbon atoms, Cl or Br and n is 0 or an integer form 1 to about 125. R 5 is an aromatic or heteroaromatic containing group, said colorants being resistant to stannous octanoate, being characterized as having improved brightness and which have functionality through reactive substituents thereof.
Inventors
- 👤 Edward W. Kluger
- 👤 Patrick D. Moore
- 👤 Joe T. Burchette
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 18:15
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/30; C08G18/38; C08G18/3819; C08G18/3836; C08G18/40; C08G18/48; C08G18/50; C08G18/5021; C08G18/5033; C08G2120/00
Claims Analysis
Total Claims: 15
Claim 1
Independent Claim
207 words
A process for coloring polyurethane resins made by a polyaddition reaction of a polyol and an isocyanate, which comprises adding to the reaction mixture before or during the polyaddition reaction a reactive coloring agent suitable for incorporation into the resin with the formation of covalent bonds, said coloring agent having the formula: ##STR26## wherein R 1 is selected from H, a lower alkyl group containing from 1 to about 10 carbon atoms, CH 2 Cl, CH 2 Br, CH 2 OH, phenyl or ##STR27## where R 6 is H or a lower alkyl group containing from 1 to about 9 carbon atoms; R 2 is selected from OH, NH 2 or SH; R 3 is selected from a lower alkyl group containing from 1 to about 9 carbon atoms, cyanoalkyl, acetoxyalkyl or ##STR28## wherein R 1 and R 2 are as given above; R 4 is H, CF 3 , a lower alkyl group containing from 1 to about 9 carbon atoms, Cl or BR and n is 0 or an integer from 1 to about 125; and R 5 is an aromatic or heteroaromatic containing group, said colorants being resistant to stannous octanoate, being characterized as having improved brightness which have functionality through reactive substituents thereof.
Claim 2
Dependent Claim
207 words
A process for coloring polyurethane resins made by a polyaddition reaction of a polyol and an isocyanate, which comprises adding to the reaction mixture before or during the polyaddition reaction a reactive coloring agent suitable for incorporation into the resin with the formation of covalent bonds, said coloring agent having the formula: ##STR26## wherein R 1 is selected from H, a lower alkyl group containing from 1 to about 10 carbon atoms, CH 2 Cl, CH 2 Br, CH 2 OH, phenyl or ##STR27## where R 6 is H or a lower alkyl group containing from 1 to about 9 carbon atoms; R 2 is selected from OH, NH 2 or SH; R 3 is selected from a lower alkyl group containing from 1 to about 9 carbon atoms, cyanoalkyl, acetoxyalkyl or ##STR28## wherein R 1 and R 2 are as given above; R 4 is H, CF 3 , a lower alkyl group containing from 1 to about 9 carbon atoms, Cl or BR and n is 0 or an integer from 1 to about 125; and R 5 is an aromatic or heteroaromatic containing group, said colorants being resistant to stannous octanoate, being characterized as having improved brightness which have functionality through reactive substituents thereof.
Claim 3
Dependent Claim
13 words
The process as defined in claim 1 wherein the polyurethane is a foam.
Claim 4
Dependent Claim
35 words
The process as defined in claim 1 wherein the colorant is given by the formula: ##STR29## wherein R 1 , R 3 , R 5 and n have the values set forth in claim 1.
Claim 5
Dependent Claim
42 words
The process as defined in claim 1 wherein the colorant is given by the formula: ##STR30## wherein R 1 is H or methyl, R 5 is as defined in claim 1, and w+x+y+z is a number of from 0 to about 32.
Claim 6
Dependent Claim
15 words
The process as defined in claim 1 wherein the polyurethane resin contains a flame retardant.
Claim 7
Dependent Claim
70 words
The process as defined in claim 1 wherein the coloring agent is at least one coloring agent selected from coloring agents of the formula ##STR31## wherein R 1 and R 3 have the values set forth in claim 1, and wherein R 5 is selected from: 2-chloro-4-methylsulfonylphenyl, 3,5-dicyano-4-methylthiophenyl, 4-chlorobenzothiazolyl, 4-methylbenzothiazolyl, 4-phenyl-thiadiazolyl, 2,6-dichlorophenyl, N,N-bis-hydroxyethylsulfonamidophenyl, 3,5-dicarboethoxy-4-methylthiophenyl, 3,5-dicarbomethoxy-4-methylthiophenyl, 3-carboethoxy-4-methyl-5-cyanothiophenyl, 3-carbomethoxy-4-methyl-5-cyanothiophenyl, 3-cyano-4,5-tetramethylene-thiophenyl, 3-carbomethoxy-5-isobutyrylthiophenyl, 3-carboethoxy-4-methyl-5-phenylamidothiophenyl, 3-cyano-4-methyl-5-acetylthiophenyl, 5-ethylthiothiadiazolyl, thiazolyl, 4-methylthiazolyl, 3-carboethoxy-4-methyl-5-cyanothiophenyl, 2-chloro-5-trifluoromethylphenyl, 2-trifluoromethyl-4-chlorophenyl, 2-trifluoromethylphenyl, 4-trifluoromethylphenyl, 3,5-bis-trifluoromethylphenyl.
Claim 8
Dependent Claim
68 words
The process as defined in claim 1 wherein the coloring agent is at least one coloring agent selected from coloring agents of the formula: ##STR32## wherein R 1 is H or methyl, and w+x+y+z equals 0 to 32; and wherein R 5 is selected from: 2-chloro-4-methylsulfonylphenyl, 3,5-dicyano-4-methylthiophenyl, 4-chlorobenzothiazolyl, 4-methylbenzothiazolyl, 4-phenylthiadiazolyl, 2,6-dichlorophenyl, N,N-bis-hydroxyethylsulfonamidophenyl, 3,5-dicarboethoxy-4-methylthiophenyl, 3,5-dicarbomethoxy-4-methylthiophenyl, 3-carboethoxy-4-methyl-5-cyanothiophenyl, 3-carbomethoxy-4-methyl-5-cyanothiophenyl, 3-cyano-4,5-tetramethylenethiophenyl, 3-carbomethoxy-5-isobutyrylthiophenyl, 3-carboethoxy-4-methyl-5-phenylamidothiophenyl, 3-cyano-4-methyl-5-acetylthiophenyl, 5-ethylthiothiadiazolyl, thiazolyl, 4-methylthiazolyl, 3-carboethoxy-4-methyl-5-cyanothiophenyl, 2-chloro-5-trifluoromethylphenyl, 2-trifluoromethyl-4-chlorophenyl, 2-trifluoromethylphenyl, 3,5-bis-trifluoromethylphenyl.
Claim 9
Dependent Claim
182 words
A colored polyurethane resin which comprises the reaction product of a polyol and an isocyanate and which further includes a covalently bound coloring agent having the formula: ##STR33## wherein R 1 is selected from H, a lower alkyl group containing from 1 to about 10 carbon atoms, CH 2 Cl, CH 2 Br, CH 2 OH, phenyl or ##STR34## where R 6 is H or a lower alkyl group containing from 1 to about 9 carbon atoms, R 2 is selected from OH, NH 2 or SH; R 3 is selected from a lower alkyl group containing from 1 to about 9 carbon atoms, cyanoalkyl, acetoxyalkyl or ##STR35## wherein R 1 and R 2 are as given above; R 4 is H, CF 3 , a lower alkyl group containing from 1 to about 9 carbon atoms, Cl or Br and n is 0 or an integer from 1 to about 125; R 5 is an aromatic or heteroaromatic containing group, said colorants being resistant to stannous octanoate, being characterized as having improved brightness and which have functionality through reactive substituents thereof.
Claim 10
Dependent Claim
182 words
A colored polyurethane resin which comprises the reaction product of a polyol and an isocyanate and which further includes a covalently bound coloring agent having the formula: ##STR33## wherein R 1 is selected from H, a lower alkyl group containing from 1 to about 10 carbon atoms, CH 2 Cl, CH 2 Br, CH 2 OH, phenyl or ##STR34## where R 6 is H or a lower alkyl group containing from 1 to about 9 carbon atoms, R 2 is selected from OH, NH 2 or SH; R 3 is selected from a lower alkyl group containing from 1 to about 9 carbon atoms, cyanoalkyl, acetoxyalkyl or ##STR35## wherein R 1 and R 2 are as given above; R 4 is H, CF 3 , a lower alkyl group containing from 1 to about 9 carbon atoms, Cl or Br and n is 0 or an integer from 1 to about 125; R 5 is an aromatic or heteroaromatic containing group, said colorants being resistant to stannous octanoate, being characterized as having improved brightness and which have functionality through reactive substituents thereof.
Claim 11
Dependent Claim
13 words
The colored resin as defined in claim 8 wherein the resin is foamed.
Claim 12
Dependent Claim
56 words
The colored resin as defined in claim 8 wherein the coloring agent has the formula: ##STR36## wherein R 1 is selected from H, or methyl, R 3 is selected from a lower alkyl group containing from 1 to about 9 carbon atoms, cyanoalkyl, acetoxyalkyl or ##STR37## and R 5 is an aromatic or heteroaromatic containing group.
Claim 13
Dependent Claim
43 words
The colored resin as defined in claim 8 wherein the coloring agent has the formula: ##STR38## wherein R 1 is H or methyl, R 5 is an aromatic or heteromatic containing group and w+x+y+z is a number of from 0 to about 32.
Claim 14
Dependent Claim
38 words
The colored resin defined in claim 10 wherein R 5 is selected from: 2-chloro-4-methylsulfonylphenyl, 3,5-dicyano-4-methylthiophenyl, 4-chlorobenzothiazolyl, 4-methylbenzothiazolyl, 4-phenylthiadiazolyl, 2,6-dichlorophenyl, N,N-bis-hydroxyethylsulfonamidophenyl, 3,5-dicarbomethoxy-4-methylthiophenyl, 3,5-dicarbomethoxy-4-methylthiophenyl, 3-carbomethoxy-4-methyl-5-cyanothiophenyl, 3-carbomethoxy-4-methyl-5-cyanothiophenyl, 3-cyano-4,5-tetramethylenethiophenyl, 3-carbomethoxy-5-isobutyrylthiophenyl, 3-carboethoxy-4-methyl-5-phenylamidothiophenyl, 3-cyano-4-methyl-5-acetylthiophenyl, 5-ethylthiothaidiazolyl, thiazolyl, 4-methylthiazolyl, 3-carboethoxy-4-methyl-5-cyanothiophenyl, 2-chloro-5-trifluoromethylphenyl, 2-trifluoromethyl-4-chlorophenyl, 2-trifluoromethylphenyl, 4-trifluoromethylphenyl, and 3,5-bis-trifluoromethylphenyl.
Claim 15
Dependent Claim
39 words
The colored resin defined in claim 11 wherein R 5 is selected from: 2-chloro-4-methylsulfonylphenyl, 3,5-dicyano-4-methylthiophenyl, 4-chlorobenzothiazolyl, 4-methylbenzothiazolyl, 4-phenylthiadiazolyl, 2,6-dichlorophenyl, N,N-bis-hydroxyethylsulfonamidophenyl, 3,5-dicarboethoxy-4-methylthiophenyl, 3,5-dicarbomethoxy-4-methylthiophenyl, 3-carboethoxy-4-methyl-5-cyanothiophenyl, 3-carbomethoxy-4-methyl-5-cyanothiophenyl, 3-cyano-4,5-tetramethylenethiophenyl, 3-carbomethoxy-5-isobutyrylthiophenyl, 3- carboethoxy-4-methyl-5-phenylamidothiophenyl, 3-cyano-4-methyl-5-acetylthiophenyl, 5-ethylthiothiadiazolyl, thiazolyl, 4-methylthiazolyl, 3-carboethoxy-4-methyl-5-cyanothiophenyl, 2-chloro-5-trifluoromethylphenyl, 2-trifluoromethyl-4-chlorophenyl, 2-trifluoromethylphenyl, 4-trifluoromethylphenyl, and 3,5-bis-trifluoromethylphenyl.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1991-06-14 | 1991-12-14 | 1992-06-14 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1995-06-14 | 1995-12-14 | 1996-06-14 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1999-06-14 | 1999-12-14 | 2000-06-14 | $7700.00 | Window Closed / Lapsed |