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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16476생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/16476

반응식

참여 물질

역할이름HCID투입량
반응물2,2,3,3-Tetrafluoro-1-propanolHCID 6441—
반응물Sodium hydrideHCID 24758—
반응물4-FluorobenzaldehydeHCID 68023—
반응물Sodium BicarbonateHCID 516892—
용매DimethylformamideHCID 6228—
생성물4-(2,2,3,3-Tetrafluoropropoxy)benzaldehydeHCID 1174662171.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737145B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d0d4560a215a435782acb8abb2ffed6a
출처 메모uspto-grants-2010_06