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HRID 16476Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/16476

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,2,3,3-Tetrafluoro-1-propanolHCID 6441—
EduktSodium hydrideHCID 24758—
Edukt4-FluorobenzaldehydeHCID 68023—
EduktSodium BicarbonateHCID 516892—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(2,2,3,3-Tetrafluoropropoxy)benzaldehydeHCID 1174662171,3%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737145B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-d0d4560a215a435782acb8abb2ffed6a
Quellennotizuspto-grants-2010_06