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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345497생성일: 2026년 10월 26일

Hydrochloric Acid → 1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanone

https://huagongshe.com/reaction/345497

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Pyrrolidine, hydrochloride (1:1)HCID 212848—
반응물1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-1-butanoneHCID 14994236—
용매IsopropanolHCID 3776—
생성물1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanoneHCID 1407133462.8%

반응 단계

A mixture of 1-(4-methoxy-5,6,7,8-tetrahydro-1-naphthyl)-1-butanone (2.50g), paraformaldehyde (0.42g), pyrrolidine hydrochloride (1.51g), and hydrochloric acid (0.2 ml) in isopropyl alcohol (7 ml) was refluxed for 15 hrs. The reaction mixture was evaporated in vacuo to give the residue. The residue was partitioned into water and ethyl ether. The aqueous layer, was extracted, neutralized with ammonia water, and then extracted with ethyl ether. The organic layer was dried over anhydrous magnesium sulfate. The mixture was filtered and the filtrate was evaporated in vacuo to give 1-(4-methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanone (2.13 g, Yield: 62.8 %) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05057535
출처 데이터셋uspto-grants-1991_10
ORD IDord-c8f0fe61614e40adb00ef055c2d4b977
출처 메모uspto-grants-1991_10