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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075546Generated: November 2, 2026

Tetrahydrofuran → 1-Fluoro-5-methoxynaphthalene

https://huagongshe.com/reaction/2075546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTetrafluoroboric acidHCID 28118—
Reactant5-methoxynaphthalen-1-amineHCID 235548—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHCID 178462726HCID 178462726—
Product1-Fluoro-5-methoxynaphthaleneHCID 1233639030%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A stirred mixture of 6.8 g of 5-amino-1-methoxynaphthalene, 57 ml THF and 74 ml of 48-50% HBF4 was cooled in an ice/salt bath. To the stirred suspension was added dropwise a solution of 3.00 g of sodium nitrite in 6 ml of water. The mixture was stirred at 0-5° C. for 30 minutes after which 300 ml of ether was added. The mixture was stirred at 0-5° C. for 45 minutes after which it was filtered and the residue washed three times with dry ether. The resulting dark red solid was air dried overnight to yield 12.2 g. The material was dissolved in 70 ml of 1-ethyl-3-methylimidazolium tetrafluoroborate and heated at 70-80° C. for 2 h (gas evolution was observed). The mixture was allowed to cool to room temperature, extracted twice with ether, washed with brine, dried (magnesium sulphate), filtered and concentrated to an oil. The material was dissolved in dichloromethane and flash chromatographed on silica gel, eluting with ethyl acetate/heptane to provide 2.08 g (30%) of 5-fluoro-1-methoxynaphthalene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919628B2
Source datasetuspto-grants-2011_04
ORD IDord-7eaaa9a87031421a871ccb534db18be6
Source noteuspto-grants-2011_04