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HRID 40408作成日:2026年10月24日

Bromobenzene → 9-bromo-13,13-dimethyl-6,11-diphenyl-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diol

https://huagongshe.com/ja/reaction/40408

反応式

関与物質

役割名称HCID仕込み量
反応物BromobenzeneHCID 7961—
反応物TetrahydrofuranHCID 8028—
反応物9-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dioneHCID 58175293—
反応物ButyllithiumHCID 178418339—
生成物9-bromo-13,13-dimethyl-6,11-diphenyl-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diolHCID 6738676763%

反応手順

Bromobenzene (8.5 g, 0.054 mol) was placed in a flask, and THF (200 ml) was added thereto. After dissolution, n-BuLi (38.4 ml, 0.06 mol) was gradually added at −780, and the reaction mixture was stirred for one hour at a maintained temperature. Then, 9-bromo-13,13-dimethyl-6H-indeno[1,2-b]anthracene-6,11(13H)-dione (10 g, 0.024 mol) was added and the reaction mixture was stirred at room temperature for 12 hours. After the reaction was terminated, the reaction solution was washed with distilled water, extracted with ethyl acetate, and purified by column chromatography to give 9-bromo-13,13-dimethyl-6,11-diphenyl-11,13-dihydro-6H-indeno[1,2-b]anthracene-6,11-diol (8.5 g, yield=63%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08525158B2
出典データセットuspto-grants-2013_09
ORD IDord-14aad029301941c69d94abba4b869465
出典メモuspto-grants-2013_09