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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341755Generated: November 2, 2026

3-Nitrobenzenesulfonyl chloride → Benzenesulfonyl fluoride, 3-nitro-

https://huagongshe.com/reaction/341755

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrobenzenesulfonyl chlorideHCID 8476—
ReactantPotassium FluorideHCID 522689—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductBenzenesulfonyl fluoride, 3-nitro-HCID 6768386.4%

Reaction Steps

3-Nitrobenzenesulphonyl chloride (10 g) was dissolved in 1,4-dioxane (30 ml) and stirred at room temperature. To this solution was added a solution of potassium fluoride (3.9 g) in water (5 ml) and the stirring continued at room temperature for 5 hours. The reaction mixture was allowed to stand at room temperature overnight and was poured into ice/water. The product was extracted into dichloromethane, the solvent was dried (MgSO4) and evaporated under reduced pressure to give the title compound (8 g). This material was sufficiently pure for the next stage of the synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856273
Source datasetuspto-grants-1999_01
ORD IDord-b6aef9a995ae42ac81fe40f748cce905
Source noteuspto-grants-1999_01