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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 461560생성일: 2026년 10월 24일

Methanesulfonic Acid → 3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole

https://huagongshe.com/ko/reaction/461560

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물(2,4-Difluoro-phenyl)-hydrazineHCID 588958—
반응물Cyclohexanone, 4-(1-piperidinyl)-HCID 12361785—
용매EthanolHCID 702—
생성물3-(1-Piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazoleHCID 12361824—

반응 단계

A solution of 10.2 g. of 4-(1-piperidyl)-cyclohexanone, 8.1 g. of 2,4-difluorophenylhydrazine, and 11 g. of methanesulfonic acid in 100 ml. of absolute ethyl alcohol was heated under reflux for 12 hours, cooled, filtered, and the filtrate was evaporated to dryness under reduced pressure. The residue was treated in ether with 10% potassium hydroxide solution and the ether extract was washed with water, dried, and treated with hydrogen chloride in ethyl alcohol (excess HCl was avoided). The resulting gummy precipitate was separated by decantation and suspended in boiling isopropyl alcohol. The hot mixture was filtered to give, after recrystallization from absolute ethyl alcohol, 4.5 g. of 3-(1-piperidyl)-6,8-difluoro-1,2,3,4-tetrahydrocarbazole hydrochloride, m.p. > 290° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04062864
출처 데이터셋uspto-grants-1977_12
ORD IDord-babb356db7d24e0ebcc7209ba8042f2f
출처 메모uspto-grants-1977_12