HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841951Generated: October 26, 2026
Ethanol → Benzenesulfonamide, 4-amino-N-[2-(4-morpholinyl)ethyl]-
https://huagongshe.com/reaction/1841951
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N-(2-Morpholin-4-yl-ethyl)-4-nitro-benzenesulfonamide | HCID 743362 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzenesulfonamide, 4-amino-N-[2-(4-morpholinyl)ethyl]- | HCID 120569 | 78% |
Reaction Steps
N-(2-Morpholin-4-yl-ethyl)-4-nitro-benzenesulfonamide (0.14 g, 0.45 mmol) was suspended in a 5:1 mixture of ethanol and water (3 ml). To this solution was added iron powder (0.13 g, 2.25 mmol) followed by saturated ammonium chloride solution (0.1 ml) and the mixture was stirred at room temperature for 18 hours. After this time, the reaction mixture was filtered through a pad of celite, the celite was washed with ethanol (10 ml) and ethyl acetate (50 ml) and the solution was concentrated under vacuum. The resulting residue was partitioned between DCM (50 ml) and water (20 ml), the organic layer was separated, dried with MgSO4, filtered and concentrated to afford the title compound (0.1 g, 78% yield) as a brown solid. Tr=0.35 min, m/z (ES+) (M+H)+ 285.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946197B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-4ac684ae0b794e45a27c19eac27c0c9e |
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| Source note | uspto-grants-2015_02 |
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