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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Dichlorobenzoyl chlorideHCID 66645—
Reactant(1E)-2-(4-Chlorophenyl)ethenesulfonamideHCID 6212331—
Solvent1,4-DioxaneHCID 31275—
Product(E)-2-(4-chloro-phenyl)-ethenesulfonic acid 2,4-dichloro-benzoylamideHCID 1560277729%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208526B2
Source datasetuspto-grants-2007_04
ORD IDord-4f7566e8918543c5a3dd5465ddcccdda
Source noteuspto-grants-2007_04