HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272356Generated: November 2, 2026
Hydrochloric Acid → (E)-2-(4-chloro-phenyl)-ethenesulfonic acid 2,4-dichloro-benzoylamide
https://huagongshe.com/reaction/1272356
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Dichlorobenzoyl chloride | HCID 66645 | — |
| Reactant | (1E)-2-(4-Chlorophenyl)ethenesulfonamide | HCID 6212331 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (E)-2-(4-chloro-phenyl)-ethenesulfonic acid 2,4-dichloro-benzoylamide | HCID 15602777 | 29% |
Reaction Steps
To a solution of (E)-2-(4-chloro-phenyl)-ethenesulfonic acid amide (65 mg, 0.3 mmol) in 1,4-dioxane (1.5 ml) was added potassium carbonate (83 mg, 0.6 mmol) followed by 2,4-dichlorobenzoyl chloride (63 μL, 0.45 mmol). The reaction was heated at 80° C. for 16 hours then allowed to cool to room temperature whereupon 1N HCl (2 ml) was added. The mixture was extracted with ethyl acetate (2 ml), the organics were dried with MgSO4 and washed with ethyl acetate (0.4 ml). The mixture was concentrated in vacuo and the resultant residue was purified by preparative HPLC to afford (E)-2-(4-chloro-phenyl)-ethenesulfonic acid 2,4-dichloro-benzoylamide (33.6 mg, 29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208526B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-4f7566e8918543c5a3dd5465ddcccdda |
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| Source note | uspto-grants-2007_04 |
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