Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436495Generated: October 25, 2026

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

https://huagongshe.com/reaction/436495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDiethylammonium chlorideHCID 10197650—
Reactant1-(2-Phenylbenzofuran-3-yl)ethanoneHCID 13024726—
SolventEthanolHCID 702—
SolventIsopropanolHCID 3776—
Product2-Phenyl-3-[3-(diethylamino)propionyl]benzofuranHCID 21452761—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04009184
Source datasetuspto-grants-1977_02
ORD IDord-ae2794e25b984ca29a251a1e2a2d4fdd
Source noteuspto-grants-1977_02