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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2-Fluoro-5-(4-methoxy-benzoyl)-benzenesulfonamide | HCID 44235278 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Amino-5-(4-methoxy-benzoyl)-benzenesulfinamide | HCID 66850637 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975439B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-b4aba0c687b845b59f6cd8f58100ff60 |
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| Source note | uspto-grants-2015_03 |
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