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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(4-Chlorophenyl)-4-fluorobenzenesulfonamide | HCID 341407 | 58% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312358B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-f396663401d6401e9f317f5031fbc68e |
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| Source note | uspto-grants-2007_12 |
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