Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810151Generated: November 3, 2026

Ammonium → 2-Fluoro-5-(4-methoxy-benzoyl)-benzenesulfonamide

https://huagongshe.com/reaction/1810151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniumHCID 223—
Reactant2-Fluoro-5-(4-methoxy-benzoyl)-benzenesulfonyl chlorideHCID 58107447—
SolventDichloromethaneHCID 6344—
Product2-Fluoro-5-(4-methoxy-benzoyl)-benzenesulfonamideHCID 4423527832%

Reaction Steps

To a solution of 2-fluoro-5-(4-methoxy-benzoyl)-benzenesulfonyl chloride (0.45 g, 1.0 mmol) in methylene chloride is added aqueous ammonium solution (1 mL). The reaction mixture is stirred for 10 min at room temperature. The solvent is removed and the residue is redissolved in ethyl acetate and extracted with water. The organic layers are washed with a saturated sodium chloride solution, dried with magnesium sulfate, and concentrated in vacuo. The residue is recrystallized with methylene chloride-hexane to give 100 mg (32% yield) of the title compound as pale yellow solid. 1 NMR (CDCl3): δ 8.40 (m, 1H), 8.05 (m, 1H), 7.80 (d, J=8 Hz, 2H), 7.32 (t, 1H), 7.00 (d, J=8 Hz, 2H), 5.15 (s, 1H), 3.90 (s, 3H). Analytics calculated for C14H12FNO4S: C, 54.36; H, 3.91; N, 4.53. Found: C, 53.89; H, 3.50; N, 4.50.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362063B2
Source datasetuspto-grants-2013_01
ORD IDord-db7e65a4332b40cda05954f840d8831a
Source noteuspto-grants-2013_01