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HRID 525975作成日:2026年10月23日

4-Bromophenol → p-Bromophenyl octyl ether

https://huagongshe.com/ja/reaction/525975

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromophenolHCID 7808—
反応物1-BromooctaneHCID 8140—
反応物Potassium CarbonateHCID 11430—
溶媒DimethylformamideHCID 6228—
生成物p-Bromophenyl octyl etherHCID 14529887.4%

反応手順

4-bromophenol (10.46 g, 60.5 mmol), 1-bromooctane (15.43 g, 79.9 mmol) and potassiumcarbonate (90 g, 0.65 mol) in N,N-dimethylformamide and was heated to 90° C. for 4 h and then the potassiumcarbonate 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 hydrochloric acid (HCl), one time with water, evaporated, and purified by distillation to obtain 1-bromo-4-(octyloxy)benzene (15.1 g, 52.9 mmol) as a colourless oil.

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-cba53612026d4ccf92bb37ba1bbffbd2
出典メモuspto-grants-2016_05