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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590714Generated: November 1, 2026

Acetamide, N-[4-(2-quinolinylmethoxy)phenyl]- → 4-(Quinolin-2-ylmethoxy)aniline

https://huagongshe.com/reaction/1590714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamide, N-[4-(2-quinolinylmethoxy)phenyl]-HCID 2747568—
SolventEthanolHCID 702—
Product4-(Quinolin-2-ylmethoxy)anilineHCID 2747569—

Reaction Steps

A suspension of N-acetyl-4-(quinolin-2-yl-methoxy)aniline (Step A, 108.9 g) in 1 L of 95% ethanol containing 10M KOH (120 mL) was heated at reflux under nitrogen in a heating mantle. When the hydrolysis was complete (approx. 36 h), the reaction mixture was cooled and ethanol was partially removed under vacuum. The mixture was then diluted with water (200 mL) and the fine off-white crystals were collected and thoroughly rinsed with water. The material, after air-drying, yielded the title compound which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05204344
Source datasetuspto-grants-1993_04
ORD IDord-2199548498b2459f9c03147b65108c6b
Source noteuspto-grants-1993_04