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HRID 36723作成日:2026年10月23日

4-Aminobenzoic Acid → 2,6-Di(tertiary-butyl)-4-(4'-carboxyphenylimino)-2,5-cyclohexadien-l-one

https://huagongshe.com/ja/reaction/36723

反応式

関与物質

役割名称HCID仕込み量
反応物4-Aminobenzoic AcidHCID 978—
反応物Boron trifluorideHCID 6356—
反応物2,6-Di-t-butyl-p-benzoquinoneHCID 12867—
溶媒TetrahydrofuranHCID 8028—
生成物2,6-Di(tertiary-butyl)-4-(4'-carboxyphenylimino)-2,5-cyclohexadien-l-oneHCID 15294543—

反応条件

温度20 °C

反応手順

A mixture of 22 g (0.10 mole) of 2,6-di(tertiary-butyl)-p-benzoquinone, 13.7 g (0.10 mole) of 4-aminobenzoic acid, 175 ml of tetrahydrofuran and 1 ml of boron trifluoride: diethyl ether complex was heated on a steam bath for 1.25 hours. The mixture was allowed to cool to about 20° C. over 16 hours under a nitrogen atmosphere. Evaporation provided a solid which was washed with hexane and recrystallized from ethanol to provide orange solid 2,6-di(tertiary-butyl)-4-(4'-carboxyphenylimino)-2,5-cyclohexadien-1-one, m.p. 305°-309° C. Analysis: Calculated for C21H25NO3 : % C, 74.3; % H, 7.4; % N, 4.1; Found: % C, 74.2; % H, 7.4; % N, 4.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05416113
出典データセットuspto-grants-1995_05
ORD IDord-62950ad97ad94a8d8b0720b1d8dc0bc7
出典メモuspto-grants-1995_05