HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390156Generated: October 30, 2026
4-(methylsulfonyl)-2-nitro-1-[(1E)-prop-1-en-1-yl]benzene → 5-(methylsulfonyl)-2-[(1E)-prop-1-en-1-yl]aniline
https://huagongshe.com/reaction/2390156
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(methylsulfonyl)-2-nitro-1-[(1E)-prop-1-en-1-yl]benzene | HCID 58521984 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(methylsulfonyl)-2-[(1E)-prop-1-en-1-yl]aniline | HCID 58522013 | 81.4% |
Reaction Steps
A solution of 4-(methylsulfonyl)-2-nitro-1-[(1E)-prop-1-en-1-yl]benzene (Intermediate 59; 1.10 g; 4.56 mmol) in AcOH (7 ml) was treated with powdered iron (3.82 g; 68.4 mmol) and the reaction mixture was stirred at 90° C. for 25 min. Further AcOH was added (20 mL), the solid was filtered off and rinsed with EtOAc. The solvents were removed under reduced pressure, the residue was taken up in EtOAc and washed with saturated NaHCO3 solution twice the with brine. The organic phase was dried on MgSO4, filtered and concentrated under reduced pressure to give the title compound as a brown oil (784 mg, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273769B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-55328cad460c4d87b5cd0170de8399c1 |
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| Source note | uspto-grants-2012_09 |
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