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HRID 339508作成日:2026年10月24日

4-Nitrobenzaldehyde → 4-(2,2,2-Trifluoroethoxy)benzaldehyde

https://huagongshe.com/ja/reaction/339508

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrobenzaldehydeHCID 541—
反応物2,2,2-TrifluoroethanolHCID 6409—
反応物Sodium hydrideHCID 24758—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Sodium chloride; waterHCID 57417360—
生成物4-(2,2,2-Trifluoroethoxy)benzaldehydeHCID 477094643.4%

反応手順

To a stirred suspension of sodium hydride (60% dispersion in mineral oil, 0.87 g, 21.8 mmol) in DMSO (20 ml) was added trifluoroethanol (3.97 g, 39.7 mmol) at 10-15° C. under an atmosphere of argon. The reaction mixture was stirred at this temperature for 20 min then 4-nitrobenzaldehyde (3.0 g, 19.85 mmol) was added in one portion. The reaction mixture was stirred at 10-15° C. for 3 h then at room temperature for 60 h. Brine (100 ml) was added cautiously to the reaction mixture followed by extraction with Et2O (3×70 ml). The combined organic extracts were washed with water, dried (MgSO4) and the solvent removed under reduced pressure to give an oil which was purified by flash chromatography (3:1 Hexane/EtOAc) to give a yellow oil which solidified on standing at room temperature to give the title compound (1.76 g, 43%) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895313B2
出典データセットuspto-grants-2014_11
ORD IDord-8188ad2868bb4596b140c3e2cc042c02
出典メモuspto-grants-2014_11