HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079603Generated: October 25, 2026
Citric Acid → N-(4-Chlorophenyl)-3-methoxy-benzenesulfonamide
https://huagongshe.com/reaction/2079603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | 3-Methoxybenzenesulfonyl chloride | HCID 2737504 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Chlorophenyl)-3-methoxy-benzenesulfonamide | HCID 57788151 | — |
Reaction Steps
To a solution of 4-chloroaniline (400 mg, 3.13 mmol) in anhydrous dichloromethane (40 mL) were added 3-methoxybenzenesulfonyl chloride (648 mg, 3.13 mmol) followed by pyridine (297.2 mg, 3.76 mmol). The mixture was allowed to stir for 12 h at 25° C. 10% citric acid solution (20 mL) and water (20 mL) was added. The organic phase was dried (Na2SO4), and evaporated under reduced pressure yielding the title compound as solid which was used as such in the next step. Yield: 900 mg (96%). MS (m/e): 296 (M+−H); 1H-NMR (CDCl3, 400 MHz): δ 3.76 (s, 3H), 6.48 (brs, 1H), 7.0 (d, J=8.72 Hz, 2H), 7.06 (d, J=7.76 Hz, 1H), 7.21 (m, 3H), 7.32 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932269B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-bf36f5f2bdfa42f99f69fd1332a065ac |
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| Source note | uspto-grants-2011_04 |
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