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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415546Generated: October 25, 2026

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

https://huagongshe.com/reaction/1415546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-AcetoxyxantheneHCID 12543454—
Reactant1-Ethyl-3-methylaminopiperidineHCID 21482809—
SolventBenzeneHCID 241—
ProductN-methyl-N-(N-ethyl-3-piperidinyl)-9-xanthenylamineHCID 21482827—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005208
Source datasetuspto-grants-1977_01
ORD IDord-db5e2acb19934cfd9b687be4999bda80
Source noteuspto-grants-1977_01