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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77656Erstellt: 23. Oktober 2026

Acetone → 1,5-Bis(3-fluorophenyl)-1,4-pentadien-3-one

https://huagongshe.com/de/reaction/77656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktWaterHCID 962—
EduktSodium HydroxideHCID 14798—
Edukt3-FluorobenzaldehydeHCID 68009—
LösungsmittelEthanolHCID 702—
Produkt1,5-Bis(3-fluorophenyl)-1,4-pentadien-3-oneHCID 6950172242%

Reaktionsschritte

3-Fluorobenzaldehyde (1s, 0.5 ml, 4.7 mmol) and acetone (19, 0.18 ml, 2.3 mmol) were combined in ethanol (20 ml) and stirred for 10 min at room temperature. A solution of sodium hydroxide (0.29 g, 7.3 mmol) and water (15 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting mixture was filtered and chromatographed on silica gel with ethyl acetate/hexane to give a solid. The crude was recrystallized from ethanol to afford 0.26 g (42%) of yellow crystals: mp 96-97° C. [expected mp 96-97° C.]; 1H NMR: δ 7.03 (d, 2H, J=16.1 Hz), 7.09 (m, 2H), 7.35 (m, 6H), 7.67 (d, 2H, J=15.9 Hz); 13C NMR: δ 114.4, 117.5, 124.4, 126.3, 130.4, 136.9, 142.0, 162.9, 188.1; Anal. Calcd for C17H12OF2: C, 75.55; H, 4.48. Found: C, 75.26; H, 4.65.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841326B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-b896188ea0824f719c74a4f42878ee58
Quellennotizuspto-grants-2014_09