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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400595Generated: October 29, 2026

5-Fluoro-2-methylphenol → 3-Fluoro-6-methyl-2-nitrophenol

https://huagongshe.com/reaction/400595

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-methylphenolHCID 2774616—
ReactantNitronium tetrafluoroborateHCID 11073463—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-Fluoro-6-methyl-2-nitrophenolHCID 6002629568%

Reaction Steps

A stirred solution of 5-fluoro-2-methylphenol (640 mg, 5 mmol) in 20 mL of anhydrous acetonitrile was cooled to −30° C. to −40° C. and treated with nitronium tetrafluoroborate (740 mg, 5.5 mmol). After 45 minutes, the reaction mixture was diluted with 100 mL of cold water and extracted with three 50 mL portions of dichloromethane. The combined organic layers were washed with three 25 mL portions of water, dried over sodium sulfate, and concentrated in vacuo to give a reddish crystalline solid. Chromatography over SiO2 (5% ethyl acetate in hexanes) gave 0.58 g of the title product as bright yellow solid (68% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741897B2
Source datasetuspto-grants-2014_06
ORD IDord-837cc21af9e64e5591bc205f022366b6
Source noteuspto-grants-2014_06