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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 436493Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-Phenyl-3-(3-piperidinopropionyl)benzofuran

https://huagongshe.com/reaction/436493

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktFormaldehydeHCID 712—
EduktPiperidine, hydrochloride (1:1)HCID 2723721—
Edukt1-(2-Phenylbenzofuran-3-yl)ethanoneHCID 13024726—
LösungsmittelEthanolHCID 702—
LösungsmittelIsopropanolHCID 3776—
Produkt2-Phenyl-3-(3-piperidinopropionyl)benzofuranHCID 21452749—

Reaktionsschritte

To a solution of 47.2 grams of 2-phenyl-3-acetylbenzofuran in 120 milliliters of isopropanol were added 6 grams of paraformaldehyde, 29.1 grams of piperidine hydrochloride and 6 milliliters of a saturated solution of hydrogen chloride in ethanol and the mixture was heated under reflux for a period of 10 hours. The solvent was evaporated from the resulting mixture under vacuum and the residue was triturated with ethyl ether. The portion of the residue that was insoluble in ether was separated from the ether extract and was dissolved in water. The aqueous solution was then made alkaline by addition thereto of a 5% aqueous solution of sodium hydroxide and the base that thus precipitated was extracted with ethyl ether and the extract was dried by addition of anhydrous sodium sulfate thereto. Upon addition to the ether extract of a solution of hydrogen chloride in ethanol, the hydrochloride of the compound named in the heading of this example precipitated, and it was separated by suction filtration and dried. it weighed 22.7 grams and, after recrystallization from ethanol, had a melting point of 173°-174°C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04009184
Quelldatensatzuspto-grants-1977_02
ORD IDord-07e6620d822e463c9712bfec0e271c1a
Quellennotizuspto-grants-1977_02