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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582775Generated: November 1, 2026

Nitrobenzene → p-Fluoronitrobenzene

https://huagongshe.com/reaction/1582775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrobenzeneHCID 7416—
Reactant1-Fluoro-3-nitrobenzeneHCID 9823—
ReactantTetrafluoroborateHCID 26255—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
SolventBenzeneHCID 241—
SolventChlorobenzeneHCID 7964—
Productp-FluoronitrobenzeneHCID 9590—

Reaction Conditions

Temperature90 °C

Reaction Steps

A homogeneous reaction mixture was obtained in this experiment, whereas in the aforementioned fluorinations of benzene and chlorobenzene, the reaction mixtures contained suspended [(ClCN)3F]+BF4−. In order to drive the fluorination of nitrobenzene to completion, the reaction mixture was heated at 90° C. for 2 hours before it was tested with Kl solution and gave a negative result. G. C. analysis revealed the presence of only 3-fluoronitrobenzene and 2-fluoronitrobenzene with no marked change in ratio (about 2:1 ratio). Despite the presence of the 2-fluoro derivative, no evidence was obtained for the presence of 4-fluoronitrobenzene. The absence of 4-fluoronitrobenzene may have resulted from loss of this isomer during the reaction or subsequent handling operations via nucleophilic displacement of the highly mobile fluorine. In this connection, the reaction vessel became etched during the reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737525B2
Source datasetuspto-grants-2004_05
ORD IDord-f1e4f9e0b36647cfafc365d2891bfdea
Source noteuspto-grants-2004_05