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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1579509생성일: 2026년 10월 26일

2,3,4,5-Tetrahydropyridine → 2-Fluorenyl 2-pyrrolidinylmethyl ketone

https://huagongshe.com/reaction/1579509

반응식

참여 물질

역할이름HCID투입량
반응물2,3,4,5-TetrahydropyridineHCID 68161—
반응물2-AcetylfluoreneHCID 69908—
반응물1-PyrrolineHCID 79803—
반응물2-AcetyldibenzofuranHCID 293028—
생성물2-Fluorenyl 2-pyrrolidinylmethyl ketoneHCID 12300793—

반응 단계

Following essentially the same procedure as in Example XI above, but substituting 2-acetylfluorene for the 2-acetyldibenzofuran above and substituting 1-pyrroline as the trimer for the 2,3,4,5-tetrahydropyridine (as α-tripiperidein) above results in the formation of 2-fluorenyl 2-pyrrolidinylmethyl ketone as the hydrochloride salt, and which when recrystallized from isopropyl alcohol has a M.P. of 234-44°C. (dec.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03931155
출처 데이터셋uspto-grants-1976_01
ORD IDord-fb20cab4092b4b5e843807665404280b
출처 메모uspto-grants-1976_01