HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399477Generated: October 27, 2026
Benzenesulfonyl chloride → 2'-Chloro-4'-nitrobenzenesulfonanilide
https://huagongshe.com/reaction/399477
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 2-Chloro-4-nitroaniline | HCID 8492 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2'-Chloro-4'-nitrobenzenesulfonanilide | HCID 231836 | — |
Reaction Steps
A mixture of 2-chloro-4-nitroaniline (4.33 g), benzenesulphonyl chloride (3.25 ml) and pyridine (2.5 ml) was stirred and heated to 100° C. for 18 hours. The mixture was cooled to ambient temperature and partitioned between methylene chloride and 2M aqueous hydrochloric acid. The organic phase was washed with water, dried and evaporated. The residue was recrystallised from ethyl acetate to give N-(2-chloro-4-nitrophenyl)benzenesulphonamide (6.07 g), m.p. 155°-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05821246 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-c466971758344711aafc5413143c01f3 |
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| Source note | uspto-grants-1998_10 |
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