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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466795Generated: October 30, 2026

Phenol → 2-Fluoro-4-(1,1,2,2-tetrafluoroethoxy)nitrobenzene

https://huagongshe.com/reaction/466795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTetrafluoroethyleneHCID 8301—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-Fluoro-4-(1,1,2,2-tetrafluoroethoxy)nitrobenzeneHCID 1472169310.6%

Reaction Steps

After dissolving 1.15 g of 3-fluoro-4-nitrophenol in 10 ml of dioxane, the resulting solution was violently stirred at about 60° C. for 15 minutes under the stream of a tetrafluoroethylene gas in large excess of said phenol. After quickly adding 0.04 g of potassium hydroxide, the solution was violently stirred for 2 hours under the same condition. The reaction solution was cooled, and after adding water, extracted with two 100-ml portions of diethyl ether. The ether layers were combined, dried and concentrated to obtain a yellow oily product as a residue. This oily product was subjected to chromatography on silica gel to obtain 0.20 g of 2-fluoro-4-(1,1,2,2-tetrafluoroethoxy)nitrobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157155
Source datasetuspto-grants-1992_10
ORD IDord-5f1b1da6dd1f417e8ad0650c0af17fec
Source noteuspto-grants-1992_10