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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630320Generated: October 26, 2026

p-Fluoronitrobenzene → 1-(2,2,3,3,4,4,4-Heptafluorobutoxy)-4-nitrobenzene

https://huagongshe.com/reaction/630320

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantHeptafluorobutanolHCID 9776—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1-(2,2,3,3,4,4,4-Heptafluorobutoxy)-4-nitrobenzeneHCID 17828877—

Reaction Steps

A solution of 2,2,3,3,4,4,4-heptafluorobutanol (5.7 g, 28.5 mmol) in DMF (100 mL) was stirred and cooled to −5° C. as sodium hydride (0.72 g, 30 mmol) was added. After 1 h at −5° C., the reaction was treated with 4-fluoronitrobenzene (4.1 g, 29 mmol). The reaction was allowed to warm to ambient temperature, concentrated, and slurried in methylene chloride (200 mL). The slurry was washed with an 1 N aqueous potassium hydroxide solution (2×) and brine solution, dried over basic alumina, treated with charcoal, filtered, and concentrated to give 4-(2′,2′,3′,3′,4′,4′,4′-heptafluorobutanoxy)nitrobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315509B2
Source datasetuspto-grants-2016_04
ORD IDord-62eae897f7904a0d93674d4af17a9095
Source noteuspto-grants-2016_04