Oxazine compound, composition and cured product
US-10399312-B2 · Sep 3, 2019 · US
US10144716B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10144716-B2 |
| Application number | US-201515532576-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 7, 2015 |
| Priority date | Dec 5, 2014 |
| Publication date | Dec 4, 2018 |
| Grant date | Dec 4, 2018 |
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This invention relates to a polybenzoxazine precursor and a method of preparing the same, and more particularly, to a polybenzoxazine precursor which includes benzoxazine obtained by reacting a phenol novolak resin with an aldehyde compound and allylamine and diaminodiphenylmethane as an amine compound, and to a method of preparing the same. The polybenzoxazine precursor may serve to prepare a hardened material having excellent thermal and electrical characteristics and dimensional stability. Accordingly, the polybenzoxazine precursor may be available for use in a copper clad laminate, a semiconductor encapsulant, a printed circuit board, an adhesive, a paint, and a mold.
Opening claim text (preview).
The invention claimed is: 1. A polybenzoxazine precursor comprising: a benzoxazine compound represented by the following Chemical Formula 1 so that a content of the benzoxazine compound of the following Chemical Formula 1 where n1 is 0, n2 is 0, and m is 1 is 5 to 50%: wherein n1 and n2 are identical or different and are each an integer of 0 to 2, and m is an integer of 1 to 6. 2. The polybenzoxazine precursor of claim 1 , wherein the precursor has a weight-average molecular weight of 1500 to 8000 g/mol and a glass transition temperature of 210° C. or higher. 3. A method of preparing a polybenzoxazine precursor of claim 1 , the method comprising: reacting a phenol novolak resin with an aldehyde compound and allylamine and diaminodiphenylmethane as an amine compound, wherein the phenol novolak resin is represented by the following Chemical Formula 2 and a component of Chemical Formula 2 where n is 0 is included in a content of 65% or more; wherein n is an integer of 0 to 2. 4. The method of claim 3 , wherein the method further comprises reacting a phenol-based compound and the aldehyde compound in a presence of an acid catalyst to obtain the phenol novolak resin. 5. The method of claim 4 , wherein the phenol novolak resin includes the aldehyde compound in a content of 0.05 to 0.3 mol based on 1 mol of the phenol-based compound, and the aldehyde compound is used in a content of 2 to 6 mol, the allylamine is used in a content of 0.5 to 1.5 mol, and the diaminodiphenylmethane is used in a content of 0.1 to 0.9 mol based on 1 mol of the phenol novolak resin. 6. A hardened material prepared from the polybenzoxazine precursor of claim 1 . 7. A polybenzoxazine, obtained by opening an oxazine ring of a polybenzoxazine precursor according to claim 1 , to perform polymerization. 8. A method of preparing a polybenzoxazine, the method comprising: hardening a polybenzoxazine precursor according to claim 1 at a temperature of 150 to 250° C. 9. The method of claim 4 , wherein the phenol novolak resin is represented by the following Chemical Formula 2 and a component of Chemical Formula 2 where n is 0 is included in a content of 65% or more: wherein n is an integer of 0 to 2.
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