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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1415546생성일: 2026년 10월 26일

9-Acetoxyxanthene → N-methyl-N-(N-ethyl-3-piperidinyl)-9-xanthenylamine

https://huagongshe.com/reaction/1415546

반응식

참여 물질

역할이름HCID투입량
반응물9-AcetoxyxantheneHCID 12543454—
반응물1-Ethyl-3-methylaminopiperidineHCID 21482809—
용매BenzeneHCID 241—
생성물N-methyl-N-(N-ethyl-3-piperidinyl)-9-xanthenylamineHCID 21482827—

반응 단계

A solution of 3.7 g. (15.4 mmoles) of 9-acetoxyxanthene and 2.2 g. (15.5 mmoles) of 1-ethyl-3-methylaminopiperidine in 80 ml. of benzene was refluxed under nitrogen for 22.5 hours. It was then cooled to room temperature, washed with aqueous sodium bicarbonate solution, and dried over potassium carbonate. After removal of solvent in vacuo, the residue was dissolved in 25 ml. of petroleum ether and filtered from a small amount of crystals. The filtrate was then concentrated in vacuo and chromatographed on silica gel (ether solvent) to give N-methyl-N-(N-ethyl-3-piperidinyl)-9-xanthenylamine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04005208
출처 데이터셋uspto-grants-1977_01
ORD IDord-db5e2acb19934cfd9b687be4999bda80
출처 메모uspto-grants-1977_01