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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415547Generated: October 31, 2026

4-Amino-1-methylpiperidine → N-(N-methyl-4-piperidinyl)-9-xanthenylamine

https://huagongshe.com/reaction/1415547

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-methylpiperidineHCID 2737531—
Reactant9-AcetoxyxantheneHCID 12543454—
SolventBenzeneHCID 241—
ProductN-(N-methyl-4-piperidinyl)-9-xanthenylamineHCID 21482845—

Reaction Steps

A solution of 4.0 g. of 9-acetoxyxanthene and 1.9 g. of 4-amino-1-methylpiperidine in 100 ml. of dry benzene was refluxed for 24 hours. The cooled solution was then washed with 5% aqueous sodium carbonate solution and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue crystallized on triturating with hexane and was recrystallized from hexane to give N-(N-methyl-4-piperidinyl)-9-xanthenylamine, m.p. 96.5°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005208
Source datasetuspto-grants-1977_01
ORD IDord-24ab40c942164b57ba21fc04a8375798
Source noteuspto-grants-1977_01