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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971315Generated: October 30, 2026

4-Chloroaniline → N-(4-Chlorophenyl)-4-fluorobenzenesulfonamide

https://huagongshe.com/reaction/971315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
SolventPyridineHCID 1049—
ProductN-(4-Chlorophenyl)-4-fluorobenzenesulfonamideHCID 34140758%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Chloroaniline (6.697 g, 52 mmol) was dissolved in pyridine (250 mL). The resulting mixture was cooled down to 0° C. 4-fluoro-benzenesulfonyl chloride (7.775 g, 40 mmol) was added in portions. The mixture was stirred between 0° C. and room temperature overnight. Solvents were evaporated to dryness. The crude oil was dissolved in ethyl acetate (150 mL) and washed with 10% HCl (2×75 mL) and brine (1×75 mL). Organic phase was dried over magnesium sulfate before filtering and removal of solvent. The resulting solid was recrystallized in cyclohexane/ethyl acetate 9:1. The desired product, e.g. 4-fluoro-N-(4-chlorophenyl)benzenesulfonamide (6.630 g, 58%), was obtained as a colorless solid, in 97.3% purity by HPLC (MaxPlot detection between 230 and 400 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312358B2
Source datasetuspto-grants-2007_12
ORD IDord-f396663401d6401e9f317f5031fbc68e
Source noteuspto-grants-2007_12