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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656336Generated: November 1, 2026

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

https://huagongshe.com/reaction/1656336

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-ylmethoxy)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, yielding the title compound which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254541
Source datasetuspto-grants-1993_10
ORD IDord-10703ce3931240db975c3b7ddd1b8056
Source noteuspto-grants-1993_10