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HRID 1084469作成日:2026年10月27日

1,4-Anthraquinone → 2-Benzylthionaphthacene-5,12-dione

https://huagongshe.com/reaction/1084469

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-AnthraquinoneHCID 69457—
反応物4-Benzylthio-2-oxo-2H-pyranHCID 14642786—
触媒Manganese dioxideHCID 14801—
溶媒1,4-DichlorobenzeneHCID 4685—
生成物2-Benzylthionaphthacene-5,12-dioneHCID 20063545—

反応条件

温度180 °C

反応手順

A mixture of 0.27 g (0.0012 mol) of 4-benzylthio-2-oxo-2H-pyrane, 0.25 g (0.0012 mol) of 1,4-anthraquinone and 0.10 g (0.0012 mol) of MnO2 in 5 ml of dichlorobenzene is heated for 24 hours under reflux (180° C.), then cooled and chromatographed over silica gel. Using cyclohexane as eluant, dichlorbenzene is first extracted, then the crude product is chromatographed with CH2Cl2. The pre-purified product is chromatographed once more, using CH2Cl2 as eluant, and the solvent is removed by evaporation. Yield: 0.09 g (20%). Melting point: 200°-203° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05004814
出典データセットuspto-grants-1991_04
ORD IDord-31ac7a23f62340e896052fd1f43801c3
出典メモuspto-grants-1991_04