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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 714173Erstellt: 23. Oktober 2026

Acetone → 1,5-Bis(2-trifluoromethylphenyl)-1,4-pentadien-3-one

https://huagongshe.com/de/reaction/714173

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktWaterHCID 962—
EduktSodium HydroxideHCID 14798—
Edukto-(Trifluoromethyl)benzaldehydeHCID 123067—
LösungsmittelEthanolHCID 702—
Produkt1,5-Bis(2-trifluoromethylphenyl)-1,4-pentadien-3-oneHCID 8543407988,7%

Reaktionsschritte

2-(Trifluoromethyl)-benzaldehyde (1w, 0.75 ml, 5.7 mmol) and acetone (19, 0.21 ml, 2.8 mmol) were combined in ethanol (20 ml) and stirred for 10 min at room temperature. A solution of sodium hydroxide (0.34 g, 8.5 mmol) and water (15 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting precipitate was filtered and recrystallized from ethanol to afford 0.92 g (87%) of a yellow solid: mp 131-133° C. [expected mp 131° C.]; 1H NMR: δ 6.99 (d, 2H, J=15.9 Hz), 7.48 (t, 2H, J=7.6 Hz), 7.56 (t, 2H, J=7.0 Hz), 7.70 (d, 2H, J=7.7 Hz), 7.77 (d, 2H, J=7.6 Hz), 8.07 (d, 2H, J=15.7 Hz); 13C NMR: δ 123.9, 126.2, 127.9, 128.8, 129.4, 129.7, 132.1, 133.7, 139.1, 188.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09187397B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-4da9f86573cc4d1ba9c30cdb355a2b03
Quellennotizuspto-grants-2015_11