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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873623Generated: October 30, 2026

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

https://huagongshe.com/reaction/873623

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. 1H 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 numberUS08975439B2
Source datasetuspto-grants-2015_03
ORD IDord-5ece9546d2dc454faff3b27f80ad36b4
Source noteuspto-grants-2015_03