Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 611091Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/611091

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
EduktFormaldehydeHCID 712—
Edukt1-(6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-6-phenylhexan-1-oneHCID 19600041—
LösungsmittelAcetic AcidHCID 176—
Produkt1-(2-dimethylaminomethyl-6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-6-phenylhexan-1-oneHCID 19600061—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 0.403 g (1.355 mmol) of 1-(6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-6-phenylhexan-1-one in 20 ml of acetic acid, 0.15 g (1.6 mmol) of 50% aqueous dimethylamine and 0.13 g (1.6 mmol) of 37% aqueous formaldehyde were added, followed by stirring at 100° C. for 15 minutes. 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-9f1f3d3a6f2a458daae6c6bbb59d3e2b
Quellennotizuspto-grants-1999_12