Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873625Generated: October 30, 2026

Ammonia → 2-Amino-5-(4-methoxy-benzoyl)-benzenesulfinamide

https://huagongshe.com/reaction/873625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-Fluoro-5-(4-methoxy-benzoyl)-benzenesulfonamideHCID 44235278—
Solvent1,4-DioxaneHCID 31275—
Product2-Amino-5-(4-methoxy-benzoyl)-benzenesulfinamideHCID 6685063781%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-fluoro-5-(4-methoxy-benzoyl)-benzenesulfonamide (0.25 g, 0.81 mmol) dissolved in dioxane (3 mL) is added aqueous ammonia solution (1 mL). The reaction mixture is heated at 100° C. for 6 h in sealed tube and then cooled to room temperature and concentrated in vacuo. The residue is partitioned between water and ethyl acetate, and the aqueous phase is extracted with ethyl acetate three times. The combined organic extracts are washed with a saturated sodium chloride solution, dried with magnesium sulfate, and concentrated in vacuo to provide 0.2 g (81%) of the title compound as a pale yellow solid. 1H NMR (DMSO): δ 8.05 (d, J=2 Hz, 1H), 7.70 (m, 3H), 7.40 (s, 2H), 7.05 (d, J=9 Hz, 2H), 6.92 (d, J=9 Hz, 1H), 3.88 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975439B2
Source datasetuspto-grants-2015_03
ORD IDord-b4aba0c687b845b59f6cd8f58100ff60
Source noteuspto-grants-2015_03