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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 85292Erstellt: 24. Oktober 2026

Isophorone → 3-[2-(4-Dibutylamino-2-methoxyphenyl)vinyl]-5,5-dimethyl-2-cyclohexenone

https://huagongshe.com/de/reaction/85292

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsophoroneHCID 6544—
EduktEthyl AcetateHCID 8857—
EduktSodium ethoxideHCID 2723922—
Edukt4-(Dibutylamino)-2-methoxybenzaldehydeHCID 14643903—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-[2-(4-Dibutylamino-2-methoxyphenyl)vinyl]-5,5-dimethyl-2-cyclohexenoneHCID 6800896545%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

In 15 ml of tetrahydrofuran, 1.5 g (10.85 mmol) of isophorone was dissolved, and 3.4 g of sodium ethoxide (20% solution in ethanol) (10.0 mmol) was added thereto. To this mixture, 2.6 g (9.87 mmol) of 4-dibutylamino-2-methoxybenzaldehyde in tetrahydrofuran was added dropwise with heating at 50° C., and the mixture was stirred for 4.5 hours. To the mixture, 100 ml of ethyl acetate was added. Washing with a saturated saline solution, drying over anhydrous sodium sulfate, and concentration were performed. The residue was purified by silica gel column chromatography to give 1.7 g of a reddish orange oily matter (yield: 45.0%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846955B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-19e301df09d24f28bc8d5a9e1c5a6ef8
Quellennotizuspto-grants-2014_09