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HRID 436493作成日:2026年10月26日

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

https://huagongshe.com/reaction/436493

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物FormaldehydeHCID 712—
反応物Piperidine, hydrochloride (1:1)HCID 2723721—
反応物1-(2-Phenylbenzofuran-3-yl)ethanoneHCID 13024726—
溶媒EthanolHCID 702—
溶媒IsopropanolHCID 3776—
生成物2-Phenyl-3-(3-piperidinopropionyl)benzofuranHCID 21452749—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04009184
出典データセットuspto-grants-1977_02
ORD IDord-07e6620d822e463c9712bfec0e271c1a
出典メモuspto-grants-1977_02