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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326047Generated: October 26, 2026

Ethanol → 4-[N-(6-chloro-2-quinolinyl)-N-methylamino]phenol

https://huagongshe.com/reaction/326047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2,6-DichloroquinolineHCID 607502—
Reactantp-(N-methylamino)phenol sulfateHCID 10198132—
SolventWaterHCID 962—
Product4-[N-(6-chloro-2-quinolinyl)-N-methylamino]phenolHCID 20461960—

Reaction Steps

A mixture of 2,6-dichloroquinoline (1.1 g; prepared according to the method of O Fischer, Chem. Ber., 35, 3683 (1902), 4-(N-methylamino)phenol sulfate (1.5 g), ethanol (5 ml) and water (20 ml) was heated under reflux for a period of 24 hours. Water (50 ml) was added to the mixture and the aqueous mixture was extracted with chloroform (2×100 ml). The chloroform extracts were dried (anhydrous MgSO4) and the solvent was evaporated to give 4-[N-(6-chloro-2-quinolinyl)-N-methylamino]phenol (1.1 g) as a dark oil. Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 8.0-6.6 and 7.2 (10H, m and d of d, quinoline, hydroxy and phenyl protons); 3.6 (3H, s, N--CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04444584
Source datasetuspto-grants-1984_04
ORD IDord-37489c974622447eb1ccd989ce18ad71
Source noteuspto-grants-1984_04