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HRID 16476作成日:2026年10月25日

2,2,3,3-Tetrafluoro-1-propanol → 4-(2,2,3,3-Tetrafluoropropoxy)benzaldehyde

https://huagongshe.com/reaction/16476

反応式

関与物質

役割名称HCID仕込み量
反応物2,2,3,3-Tetrafluoro-1-propanolHCID 6441—
反応物Sodium hydrideHCID 24758—
反応物4-FluorobenzaldehydeHCID 68023—
反応物Sodium BicarbonateHCID 516892—
溶媒DimethylformamideHCID 6228—
生成物4-(2,2,3,3-Tetrafluoropropoxy)benzaldehydeHCID 1174662171.3%

反応手順

To sodium hydride (288 mg as 55-60% mineral oil dispersion, 6 mmol) in N,N-dimethylformamide (2 mL), a solution of 2,2,3,3-tetrafluoro-1-propanol (535 μL, 6 mmol) in N,N-dimethylformamide (8 mL) was added dropwise. The reaction mixture was stirred for thirty minutes at room temperature. Then, 4-fluorobenzaldehyde (429 μL, 4 mmol) was added slowly, and the reaction was heated to 80° C. for three hours. After cooling, saturated sodium bicarbonate solution was added. The mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. Flash chromatography gave 674 mg of 4-(2,2,3,3-tetrafluoropropoxy)benzaldehyde; 1H NMR (300 MHz, CDCl3) δ 9.93 (s, 1H), 7.88 (d, 2H), 7.06 (d, 2H), 6.06 (tt, 1H), 4.44 (tt, 2H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737145B2
出典データセットuspto-grants-2010_06
ORD IDord-d0d4560a215a435782acb8abb2ffed6a
出典メモuspto-grants-2010_06