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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810153Generated: October 31, 2026

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

https://huagongshe.com/reaction/1810153

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 numberUS08362063B2
Source datasetuspto-grants-2013_01
ORD IDord-1cebe7edeb3b4567bf9d8241d5d9f233
Source noteuspto-grants-2013_01