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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351539Erstellt: 24. Oktober 2026

Triethylamine → 1-(4-Methoxycarbonylphenyl)-4-(4-n-pentyloxyphenyl)butane-1,4-dione

https://huagongshe.com/de/reaction/351539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethyl 4-FormylbenzoateHCID 15294—
Edukt1-(4-n-Pentyloxyphenyl)acroleinHCID 22713222—
Katalysator3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chlorideHCID 2833352—
LösungsmittelEthanolHCID 702—
Produkt1-(4-Methoxycarbonylphenyl)-4-(4-n-pentyloxyphenyl)butane-1,4-dioneHCID 2271322381,8%

Reaktionsschritte

A suspension of 1-(4-n-pentyloxyphenyl)acrolein (2.38 g), methyl 4-formylbenzoate (1.97 g), 3-benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride and triethylamine (0.91 ml) in ethanol (10 ml) was refluxed for 18 hours. After cooling, the solvents were removed under reduced pressure. The solids were taken up in 1N HCl and extracted with dichloromethane. The organic layer was washed successively with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was triturated with diisopropyl ether, collected by filtration and dried under reduced pressure to give 1-(4-methoxycarbonylphenyl)-4-(4-n-pentyloxyphenyl)butane-1,4-dione (3.41 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743776B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-1dfc266d3ef0430ca5d5774187bb1e33
Quellennotizuspto-grants-2004_06