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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455293Generated: October 30, 2026

4-Nitrophenol → 4-[(2-Methyl-4-quinolinyl)methoxy]benzenamine dihydrochloride

https://huagongshe.com/reaction/1455293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantSodium IodideHCID 5238—
ReactantCesium carbonateHCID 10796—
ReactantStannous ChlorideHCID 24479—
Reactant4-(Chloromethyl)-2-methylquinolineHCID 11535719—
SolventTetrahydrofuranHCID 8028—
Product4-[(2-Methyl-4-quinolinyl)methoxy]benzenamine dihydrochlorideHCID 67305537—

Reaction Steps

To a solution of 4-nitrophenol (7.2 g, 52.0 mmol) in 400 mL THF was added 4-(chloromethyl)-2-methylquinoline (10.0 g, 52.0 mmol), cesium carbonate (25.4 g, 78 mmol), and sodium iodide (451 mg, 3 mmol). The reaction was heated to reflux for 24 hr, after which the reaction was extracted from sat KH2PO4 with EtOAc×3. The combined organic layers were dried with MgSO4, filtered, and concentrated. This residue was taken up in 200 mL MeOH and refluxed with SnCl2 (156 mmol) for 18 hr after which, the solution was cooled and the reaction was extracted from disodium tartrate with EtOAc×4, the combined organic layers were dried with MgSO4, filtered, and concentrated. The residue was treated with 2 M HCl in dioxane, rotovapped, and recrystallized from EtOH/water to give 12.4 g (71%). MS found: (M+H)=265.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482372B2
Source datasetuspto-grants-2009_01
ORD IDord-68b4c31f77954b26bbd028b8105483c2
Source noteuspto-grants-2009_01