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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272363Generated: November 2, 2026

Water → (E)-2-(2-chloro-phenyl)-ethenesulfonic acid 4-bromo-2-chloro-benzoylamide

https://huagongshe.com/reaction/1272363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-(2-Chlorophenyl)ethene-1-sulfonamideHCID 11020338—
Reactant4-Bromo-2-chlorobenzoyl chlorideHCID 15592207—
Solvent1,4-DioxaneHCID 31275—
Product(E)-2-(2-chloro-phenyl)-ethenesulfonic acid 4-bromo-2-chloro-benzoylamideHCID 15603095—

Reaction Steps

Sodium hydride (60% dispersion in mineral oil) (36 mg, 0.9 mmol) was added to a solution of (E)-2-(2-chloro-phenyl)-ethenesulfonic acid amide (65 mg, 0.3 mmol) in 1,4-dioxane (1.5 mL) and the reaction mixture was shaken for 30 minutes. Crude 4-bromo-2-chloro-benzoyl chloride (114 mg, 0.45 mmol) in dioxane (0.5 mL) was added and the reaction mixture was shaken at room temperature for 18 hours. Water (0.1 mL) was added to the reaction mixture and the whole was concentrated in vacuo. The resultant residue was purified by preparative HPLC under neutral conditions to give (E)-2-(2-chloro-phenyl)-ethenesulfonic acid 4-bromo-2-chloro-benzoylamide; sodium salt (38 mg, 29% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208526B2
Source datasetuspto-grants-2007_04
ORD IDord-c48f4735e72e4660a31253ed29dcc3c7
Source noteuspto-grants-2007_04