Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988816Generated: November 2, 2026

Nitrobenzene → p-Fluoronitrobenzene

https://huagongshe.com/reaction/988816

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 KI 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 were 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 numberUS06635760B2
Source datasetuspto-grants-2003_10
ORD IDord-147f01bd25ce47d0ae74ce3fb1ff166b
Source noteuspto-grants-2003_10