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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 611176Erstellt: 26. Oktober 2026

Acetic Acid → 1-(2-ethylmethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one

https://huagongshe.com/reaction/611176

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktFormaldehydeHCID 712—
EduktN-MethylethylamineHCID 12219—
Edukt1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-oneHCID 19600145—
Produkt1-(2-ethylmethylaminomethyl-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-oneHCID 67584926—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 0.400 g (1.345 mmol) of 1-(5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl)-6-phenylhexan-1-one in 20 ml of acetic acid, 0.14 ml (1.6 mmol) of N-Ethylmethylamine and 0.13 9 (1.6 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 1 hour. After the solvent was distilled off under reduced pressure, the residual solution was alkalified with aqueous sodium hydroxide and extracted with dichloromethane 3 times. The combined organic layer was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (ethyl acetate to ethyl acetate/methanol=4/1) to yield the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05998433
Quelldatensatzuspto-grants-1999_12
ORD IDord-6b244c45fd7d4ddeab8e414b0545dfed
Quellennotizuspto-grants-1999_12