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HRID 1415546作成日:2026年10月27日

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

https://huagongshe.com/reaction/1415546

反応式

関与物質

役割名称HCID仕込み量
反応物9-AcetoxyxantheneHCID 12543454—
反応物1-Ethyl-3-methylaminopiperidineHCID 21482809—
溶媒BenzeneHCID 241—
生成物N-methyl-N-(N-ethyl-3-piperidinyl)-9-xanthenylamineHCID 21482827—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04005208
出典データセットuspto-grants-1977_01
ORD IDord-db5e2acb19934cfd9b687be4999bda80
出典メモuspto-grants-1977_01