戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 21510作成日:2026年10月26日

Water → 4-[(2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-2-(p-methoxyphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/21510

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物4-MethoxyphenolHCID 9015—
反応物Potassium CarbonateHCID 11430—
反応物2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl 3,4-dinitrophenyl etherHCID 86748711—
溶媒AcetonitrileHCID 6342—
生成物4-[(2-Chloro-alpha,alpha,alpha,6-tetrafluoro-p-tolyl)oxy]-2-(p-methoxyphenoxy)-1-nitrobenzeneHCID 8674871225.2%

反応手順

A mixture of 2-chloro-α,α,α,6-tetrafluoro-p-tolyl 3,4-dinitrophenyl ether (10.0 g, 0.026 mol), 4methoxyphenol (6.45 g, 0.052 mol) and potassium carbonate (7.26 g, 0.052 mol) in acetonitrile is refluxed for 18 hours, cooled to room temperature, poured into water and extracted with ethyl acetate. The organic extract is washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain an amber oil. Column chromatography of the oil using silica gel and a (1:4) ether/hexanes solution gives the title product as a yellow oil (3.0 g) which is identified by 1HNMR and 13CNMR spectral analyses.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424280
出典データセットuspto-grants-1995_06
ORD IDord-e3ab984d5c024708ae7185b42301c498
出典メモuspto-grants-1995_06