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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 632509Erstellt: 26. Oktober 2026

Butylamine → (1E,6E)-1,7-bis[4-(2-morpholinoethoxy)phenyl]hepta-1,6-diene-3,5-dione

https://huagongshe.com/reaction/632509

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButylamineHCID 8007—
EduktPotassium CarbonateHCID 11430—
EduktAcetylacetoneHCID 31261—
Edukt4-(2-Morpholinoethoxy)benzaldehydeHCID 3719902—
EduktBoron monoxideHCID 6327189—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelTributyl borateHCID 12712—
Produkt(1E,6E)-1,7-bis[4-(2-morpholinoethoxy)phenyl]hepta-1,6-diene-3,5-dioneHCID 11788904324%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To 2.0 g of pentane-2,4-dione were added 10.0 mL of AcOEt and 0.70 g of boron oxide, and the mixture was stirred at 70° C. for 1 hour. To the reaction mixture, 30 mL of a solution of 9.4 g of 4-(2-morpholinoethoxy)benzaldehyde in AcOEt and 10.7 mL of tributyl borate were successively added, and the mixture was stirred at the same temperature for 1 hour. To this, 0.4 mL of 1-butylamine was added, and the mixture was stirred at 70° C. for 2.5 hours and was allowed to cool back to room temperature. To the reaction mixture, 50 mL of a 10% K2CO3 aqueous solution and 30 mL of THF were added, and the mixture was stirred at room temperature for 10 minutes. The organic layer was separated, washed with saturated brine, dried over MgSO4, and concentrated. The residue was treated with 100 mL of diethyl ether to give 2.51 g of the title compound as a powder (24% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09321752B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-48d512c5912943118d34aa4458f6fa9f
Quellennotizuspto-grants-2016_04