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HRID 525979作成日:2026年10月23日

Quinizarin → 1,4-Bis(octyloxy)anthracene-9,10-dione

https://huagongshe.com/ja/reaction/525979

反応式

関与物質

役割名称HCID仕込み量
反応物QuinizarinHCID 6688—
反応物1-BromooctaneHCID 8140—
反応物Potassium CarbonateHCID 11430—
溶媒DimethylformamideHCID 6228—
生成物1,4-Bis(octyloxy)anthracene-9,10-dioneHCID 6844131737.7%

反応手順

1,4-dihydroxyanthracene-9,10-dione (5.0 g, 20.6 mmol), 1-bromooctane (10.0 g, 51.8 mmol), and potassium carbonate (37 g, 0.268 mol) was mixed in N,N-dimethylformamide and heated at 90° C. for 7 h after which the potassium carbonate was filtered off. The reaction mixture was quenched with water and extracted three times with ether. The ether was then washed three times with 1M HCl, one time with water, and evaporated to give a dark yellow solid. This solid was recrystallised in methanol to yield 1,4-bis(octyloxy)anthracene-9,10-dione (1.81 g, 3.88 mmol) as a yellow solid. 1H-NMR (CDCl3, δ): 0.89 (t, 6H), 1.2-1.4 (m, 16H), 1.53 (m, 4H), 1.93 (m, 4H), 4.10 (t, 4H), 7.30 (s, 2H), 7.71 (m, 2H), 8.16 (m, 2H) MS MALDI-TOF (m/z): 464.328

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09343198B2
出典データセットuspto-grants-2016_05
ORD IDord-555a9ae8fe2840619383765dd74b0a95
出典メモuspto-grants-2016_05