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HRID 1928517作成日:2026年10月27日

Formaldehyde → Dihydrobenzoxazine

https://huagongshe.com/reaction/1928517

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物PhenolHCID 996—
反応物Bis(aminomethyl)tricyclo[5,2,1,02,6]decaneHCID 53737527—
溶媒ChloroformHCID 6212—
生成物DihydrobenzoxazineHCID 21887592—

反応条件

温度60 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08183368B2
出典データセットuspto-grants-2012_05
ORD IDord-0c98b5027cee4fd08448c6f83a4a0314
出典メモuspto-grants-2012_05