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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742369Generated: October 30, 2026

1-Fluoro-3-nitrobenzene → HCID 19425982, compound

https://huagongshe.com/reaction/742369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Fluoro-3-nitrobenzeneHCID 9823—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178466152HCID 178466152—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 19425982HCID 19425982—

Reaction Steps

4-Acetylbenzimidazole (4.4 g, 27.5 mmol) was dissolved in dry DMSO (40 ml) and cooled. Sodium hydride (0.91 g, 80% suspension in oil) was added and the mixture was allowed to warm to room temperature. When the evolution of hydrogen had ceased 1-fluoro-3-nitrobenzene was added and the mixture was heated to 120° C. overnight. After cooling the reaction mixture was poured into ice-water and the crude product was filtered off. Purification was achieved by column chromatography on silica gel with ethyl acetate/petroleum ether (1:1) as the eluent. Yield 2.09 g, mp 175°-177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554632
Source datasetuspto-grants-1996_09
ORD IDord-aa2fe7affbd34b94b0909b74e0993050
Source noteuspto-grants-1996_09