돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 436493생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/436493

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Piperidine, hydrochloride (1:1)HCID 2723721—
반응물1-(2-Phenylbenzofuran-3-yl)ethanoneHCID 13024726—
용매EthanolHCID 702—
용매IsopropanolHCID 3776—
생성물2-Phenyl-3-(3-piperidinopropionyl)benzofuranHCID 21452749—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04009184
출처 데이터셋uspto-grants-1977_02
ORD IDord-07e6620d822e463c9712bfec0e271c1a
출처 메모uspto-grants-1977_02