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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77669Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/77669

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktWaterHCID 962—
Edukt1-NaphthaldehydeHCID 6195—
EduktSodium HydroxideHCID 14798—
LösungsmittelEthanolHCID 702—
Produkt1,5-Bis(1-naphthyl)-1,4-pentadien-3-oneHCID 59251238%

Reaktionsschritte

1-Naphthaldehyde (22, 1.36 ml, 10.0 mmol) and acetone (19, 0.37 ml, 5.0 mmol) were combined in ethanol (10 ml) and stirred for 15 min at room temperature. A solution of sodium hydroxide (0.40 g, 10.0 mmol) and water (10 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting mixture was extracted into ethyl acetate, washed with saturated sodium chloride, filtered and evaporated to afford a solid. The crude solid was recrystallized from ethyl acetate to give 0.63 g (38%) of a yellow solid: mp 132-133° C. [expected mp 128° C.]; 1H NMR: δ 7.24 (d, 2H, J=15.7 Hz), 7.57 (m, 6H), 7.92 (m, 6H), 8.28 (d, 2H, J=8.0 Hz), 8.65 (d, 2H, J=15.5 Hz); 13C NMR: δ 123.4, 125.1, 125.4, 126.2, 126.9, 128.1, 128.7, 130.7, 131.7, 132.2, 133.7, 140.3, 188.5.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841326B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-5793ccc1061342aabbd3ef45a1c777b5
Quellennotizuspto-grants-2014_09