Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | M-Xylene | HCID 7929 | — |
| Reactant | 1,3-Benzenedimethanamine | HCID 15133 | — |
| Reactant | Diglycidyl ether | HCID 16704 | — |
| Catalyst | Ethylene Glycol | HCID 174 | — |
| Catalyst | Epichlorohydrin | HCID 7835 | — |
| Product | Butyl glycidyl ether | HCID 17049 | 210% |
Reaction Steps
In the same reaction vessel as in Example 1 was fed 270 g of the modified polyamine synthesized in Production Example 1 (corresponding to the modified polyamine based on 1 mol of metaxylene, 0.125 mol of methoxypolyethylene glycol and 0.14 mol of epichlorohydrin), and then 186 g (1 mol) of 2-ethylehexyl glycidyl ether (epoxy equivalent of 186, produced by NOF Corporation, the trademark "Epiol EH") was added dropwise thereto over one hour at 80° C. in an atmosphere of nitrogen under stirring. After the completion of the dropwise addition, the reaction was carried out for one hour at a reaction temperature raised 100° C. Then, the vessel interior was cooled to 80° C., and then 231 g (1.70 mol) of metaxylylenediamine was added thereto. Then, a mixture of 307 g (0.807 mol) of epoxy resin in a liquid form of bisphenol A type (epoxy equivalent 190, produced by Yuka Shell Epoxy Co., Ltd., the trademark "Epicoat 828) with 278 g (2.1 mol) of butyl glycidyl ether (epoxy equivalent of 132, produced by NOF Corporation, the tradmark "Epiol B") was added dropwise thereto over one hour at 80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05936011 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-84ad2b812adb4ef5805b940754297e10 |
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| Source note | uspto-grants-1999_08 |
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