← Back to Patent Explorer
US4487915A Expired / Lapsed US ⏱️ 0.0 years remaining

Hydroxy aromatic oligomers containing triazine and oxazoline groups and epoxy resins prepared therefrom

Assignee: Dow Chemical Co
•
Filing: 1984-02-02
•
Granted: 1984-12-11
•
Expires: 2004-02-02
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract The subject oligomers are prepared by reacting a diphenol with a cyanogen halide in the presence of an alkaline agent. The resultant product is then reacted with an epoxy resin thereby producing a hydroxy aromatic oligomers containing triazine and oxazoline groups. An epoxy resin is then prepared by reacting the previously formed oligomers with an epihalohydrin followed by dehydrohalogenation of the resultant product.

Inventors

  • 👤 Robert E. Hefner, Jr.

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 08:22
CPC Classifications
C; C08; C08G; C08G59/00; C08G59/18; C08G59/40; C08G59/4007; C08G59/4014; C07; C07C; C07C261/00; C07C261/02; C07D; C07D251/00; C07D251/02; C07D251/12; C07D251/26; C07D251/30; C07D251/34; C08G59/02; C08G59/04; C08G59/06; C08G59/066; C08G59/20; C08G59/22; C08G59/26; C08G59/32; C08G59/3236

Claims Analysis

Total Claims: 22
Claim 1
Independent Claim 140 words
Hydroxyaromatic oligomer compositions containing both triazine and oxazoline groups prepared by reacting (A) at least one material having an average of more than one aromatic hydroxyl group per molecule with (B) at least 0.01 but not more than 0.95 moles of cyanogen halide or mixture of cyanogen halides per aromatic hydroxyl group in the presence of (C) a suitable base in a quantity of from about 0.01 to about 1.1 moles per aromatic hydroxyl group at a temperature and time sufficient to essentially complete the reaction and thereafter recovering the resultant cyanate mixture; (II) co-oligomerizing the product resulting from (I) with (D) an epoxy resin wherein the mole ratio of epoxy groups to cyanate groups is about 1:1 to about 1:100 in the presence of a suitable co-oligomerization catalyst at a temperature and time to essentially complete the co-oligomerization reaction.
Claim 2
Dependent Claim 140 words
Hydroxyaromatic oligomer compositions containing both triazine and oxazoline groups prepared by reacting (A) at least one material having an average of more than one aromatic hydroxyl group per molecule with (B) at least 0.01 but not more than 0.95 moles of cyanogen halide or mixture of cyanogen halides per aromatic hydroxyl group in the presence of (C) a suitable base in a quantity of from about 0.01 to about 1.1 moles per aromatic hydroxyl group at a temperature and time sufficient to essentially complete the reaction and thereafter recovering the resultant cyanate mixture; (II) co-oligomerizing the product resulting from (I) with (D) an epoxy resin wherein the mole ratio of epoxy groups to cyanate groups is about 1:1 to about 1:100 in the presence of a suitable co-oligomerization catalyst at a temperature and time to essentially complete the co-oligomerization reaction.
Claim 3
Dependent Claim 81 words
A hydroxyaromatic oligomer composition of claim 1 wherein (i) components (A) and (B) are present in quantities which provides from about 0.05 to about 0.55 moles of cyanogen halide or a mixture of cyanogen halides per aromatic hydroxyl group; (ii) component (C) is present in quantities which provides from about 0.05 to about 0.6 moles of base per mole of aromatic hydroxyl group; and (iii) the mole ratio of epoxy groups to cyanate groups is from about 1:10 to about 1:40.
Claim 4
Dependent Claim 56 words
A hydroxyaromatic oligomer composition of claim 2 wherein (i) component (A) is a compound represented by formulas I, II or III in the specification; (ii) component (B) is cyanogen chloride, cyanogen bromide or a mixture thereof; (iii) component (C) is a trialkylamine; and (iv) component (D) is represented by formulas IV or V in the specification.
Claim 5
Dependent Claim 18 words
A hydroxyaromatic oligomer composition of claim 3 wherein (i) component (A) is a compound represented by formula II;
Claim 6
Dependent Claim 17 words
(ii) component (C) is triethylamine; and (iii) component (D) is an epoxy resin represented by formula IV.
Claim 7
Dependent Claim 17 words
(ii) component (C) is triethylamine; and (iii) component (D) is an epoxy resin represented by formula IV.
Claim 8
Dependent Claim 74 words
A hydroxyaromatic oligomer composition of claim 4 wherein (i) in component (A) A is a divalent hydrocarbon group having from 1 to about 12 carbon atoms and n has a value of 1; and (ii) in component (D) each A is independently a divalent hdyrocarbon group having from 1 to about 12 carbon atoms, n has a value of 1 and m 2 has an average value of from about 0 to about 40.
Claim 9
Dependent Claim 41 words
A hydroxyaromatic oligomer composition of claim 5 wherein (i) in component (A), A is an isopropylidene group; and (ii) in component (D) A is an isopropylidene group and m 2 has an average value of from about 0.1 to about 20.
Claim 10
Dependent Claim 168 words
An epoxy-containing composition having an average of more than one epoxy group per molecule prepared by dehydrohalogenating the reaction product resulting from reacting an epihalohydrin with a hydroxy aromatic oligomer composition containing both triazine and oxazoline groups prepared by reacting (A) at least one material having an average of more than one aromatic hydroxyl group per molecule with (B) at least 0.01 but not more than 0.95 moles of cyanogen halide or mixture of cyanogen halides per aromatic hydroxyl group in the presence of (C) a suitable base in a quantity of from about 0.01 to about 1.1 moles per aromatic hydroxyl group at a temperature and time sufficient to essentially complete the reaction and thereafter recovering the resultant cyanate mixture; (II) co-oligomerizing the product resulting from (I) with (D) an epoxy resin wherein the mole ratio of epoxy groups to cyanate groups is about 1:10 to about 1:100 in the presence of a suitable co-oligomerization catalyst at a temperature and time to essentially complete to co-oligomerization reaction.
Claim 11
Dependent Claim 168 words
An epoxy-containing composition having an average of more than one epoxy group per molecule prepared by dehydrohalogenating the reaction product resulting from reacting an epihalohydrin with a hydroxy aromatic oligomer composition containing both triazine and oxazoline groups prepared by reacting (A) at least one material having an average of more than one aromatic hydroxyl group per molecule with (B) at least 0.01 but not more than 0.95 moles of cyanogen halide or mixture of cyanogen halides per aromatic hydroxyl group in the presence of (C) a suitable base in a quantity of from about 0.01 to about 1.1 moles per aromatic hydroxyl group at a temperature and time sufficient to essentially complete the reaction and thereafter recovering the resultant cyanate mixture; (II) co-oligomerizing the product resulting from (I) with (D) an epoxy resin wherein the mole ratio of epoxy groups to cyanate groups is about 1:10 to about 1:100 in the presence of a suitable co-oligomerization catalyst at a temperature and time to essentially complete to co-oligomerization reaction.
Claim 12
Dependent Claim 85 words
An epoxy-containing composition of claim 7 wherein (i) components (A) and (B) are present in quantities which provides from about 0.05 to about 0.55 moles of cyanogen halide or a mixture of cyanogen halides per aromatic hydroxyl group; (ii) component (C) is present in quantities which provides from about 0.05 to about 0.6 moles of base per mole of aromatic hydroxyl group; (iii) the mole ratio of epoxy groups to cyanate groups is from about 1:10 to about 1:40; and (iv) said epihalohydrin is epichlorohydrin.
Claim 13
Dependent Claim 55 words
An epoxy-containing composition of claim 8 wherein (i) component (A) is a compound represented by formulas I, II or III in the specification; (ii) component (B) is cyanogen chloride, cyanogen bromide or a mixture thereof; (iii) component (C) is a trialkylamine; and (iv) component (D) is represented by formulas IV or V in the specification.
Claim 14
Dependent Claim 34 words
An epoxy-containing composition of claim 9 wherein (i) component (A) is a compound represented by formula II; (ii) component (C) is triethylamine; and (iii) component (D) is an epoxy resin represented by formula IV.
Claim 15
Dependent Claim 73 words
An epoxy-containing composition of claim 4 wherein (i) in component (A) A is a divalent hydrocarbon group having from 1 to about 12 carbon atoms and n has a value of 1; and (ii) in component (D) each A is independently a divalent hydrocarbon group having from 1 to about 12 carbon atoms, n has a value of 1 and m 2 has an average value of from about 0 to about 40.
Claim 16
Dependent Claim 40 words
An epoxy-containing composition of claim 5 wherein (i) in component (A), A is an isopropylidene group; and (ii) in component (D) A is an isopropylidene group and m 2 has an average value of from about 0.1 to about 20.
Claim 17
Dependent Claim 22 words
A product resulting from curing an epoxy-containing composition of claim 7 with a curing quantity of a suitable catalyst and/or curing agent.
Claim 18
Dependent Claim 22 words
A product resulting from curing an epoxy-containing composition of claim 8 with a curing quantity of a suitable catalyst and/or curing agent.
Claim 19
Dependent Claim 23 words
A product resulting from curing an epoxy-containing composition of claim 9 with a curing quantity of a suitable catalyst and/or a curing agent.
Claim 20
Dependent Claim 22 words
A product resulting from curing an epoxy-containing composition of claim 10 with a curing quantity of a suitable catalyst and/or curing agent.
Claim 21
Dependent Claim 22 words
A product resulting from curing an epoxy-containing composition of claim 11 with a curing quantity of a suitable catalyst and/or curing agent.
Claim 22
Dependent Claim 22 words
A product resulting from curing an epoxy-containing composition of claim 12 with a curing quantity of a suitable catalyst and/or curing agent.

References Cited (Backward Citations)

US2810706A Cited
US2741607A Cited
US2809942A Cited
US2864805A Cited
US2971942A Cited
US3708483A Cited
US3676397A Cited
JPS5626925A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-12-11 1988-06-11 1988-12-11 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-12-11 1992-06-11 1992-12-11 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-12-11 1996-06-11 1996-12-11 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag