関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Phenol | HCID 996 | — |
| 反応物 | Bis(aminomethyl)tricyclo[5,2,1,02,6]decane | HCID 53737527 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Dihydrobenzoxazine | HCID 21887592 | — |
反応手順
One mole of 3(4),8(9),-bis(aminomethyl)tricyclo[5,2,1,02,6]decane as saturated alicyclic hydrocarbon diamine compound having a condensed ring structure, two moles of phenol as the phenol compound represented by Formula (1), as well as, 4 moles of paraformaldehyde as aldehyde compound and 1500 g of chloroform were mixed. This mixture was heated to 60° C. under stirring, and the reaction was carried out for 6 hours since chloroform started circulating. After the end of the reaction, the reaction mixture was washed with an aqueous solution of 1 N sodium hydroxide, and then rinsed with ion exchanged water. Then, after the chloroform phase was dried with anhydrous sodium sulfate, chloroform was evaporated with a rotary evaporator to obtain a bifunctional dihydro benzoxazine compound in which R14 of Formula (2) is the amino residue of 3(4),8(9),-bis(aminomethyl)tricyclo[5,2,1,02,6]decane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08183368B2 |
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| 出典データセット | uspto-grants-2012_05 |
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| ORD ID | ord-0c98b5027cee4fd08448c6f83a4a0314 |
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| 出典メモ | uspto-grants-2012_05 |
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