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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 436495Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Phenyl-3-[3-(diethylamino)propionyl]benzofuran

https://huagongshe.com/de/reaction/436495

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktFormaldehydeHCID 712—
EduktDiethylammonium chlorideHCID 10197650—
Edukt1-(2-Phenylbenzofuran-3-yl)ethanoneHCID 13024726—
LösungsmittelEthanolHCID 702—
LösungsmittelIsopropanolHCID 3776—
Produkt2-Phenyl-3-[3-(diethylamino)propionyl]benzofuranHCID 21452761—

Reaktionsschritte

To a solution of 47.2 grams of 2-phenyl-3-acetyl benzofuran in 150 milliliters of isopropanol, were added 8.4 grams of paraformaldehyde, 30.8 grams of diethylamine hydrochloride and 3 milliliters of a saturated solution of hydrogen chloride in ethanol and the mixture was heated at its boiling point under reflux for 8 hours. The solvent was then evaporated from the mixture under vacuum and the residue was triturated with water and the insoluble portion thereof was extracted therefrom with ethyl ether. The aqueous solution was made alkaline by the addition of a 5% aqueous sodium hydroxide solution and the oily base which separated was extracted with ethyl ether. After drying the ether extract over anhydrous sodium sulfate a solution of hydrogen chloride in ethanol was added thereto and the crystalline hydrochloride of the compound named in the heading of this example precipitated. The crystals thus obtained were recrystallized in a mixture of ethanol and ethyl ether. In this manner, 34.2 grams of the recrystallized hydrochloride, which had a melting point of 113°-115°C, was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04009184
Quelldatensatzuspto-grants-1977_02
ORD IDord-ae2794e25b984ca29a251a1e2a2d4fdd
Quellennotizuspto-grants-1977_02