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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737221Generated: November 1, 2026

2-Naphthol → Naphthalene, 2-(2-nitrophenoxy)-

https://huagongshe.com/reaction/1737221

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphtholHCID 8663—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
SolventTetrahydrofuranHCID 8028—
ProductNaphthalene, 2-(2-nitrophenoxy)-HCID 928048799.9%

Reaction Steps

To a stirred solution of 2-hydroxynaphthalene (5 g, 34.7 mmol) in anhydrous tetrahydrofuran was added 2-fluoronitrobenzene (4.90 g, 34.7 mmol) at room temperature. The resultant mixture was heated at reflux overnight. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure, the residue was diluted with water, the resulting mixture was extracted twice with methylene chloride and the combined extracts were dried (MgSO4). The resultant organic layer was concentrated under reduced pressure to yield 9.2 g of the title compound of Step A as an oil. Rf 0.45 (silica gel, 4:1 hexane-ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962436
Source datasetuspto-grants-1999_10
ORD IDord-6006c8c328c44bcea5b53027a34b0c78
Source noteuspto-grants-1999_10