Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Chloro-2-nitro-4-[(1E)-2-nitro-1-propen-1-yl]benzene | HCID 13776266 | — |
| Catalyst | Iron | HCID 23925 | — |
| Product | HCID 68724436 | HCID 68724436 | — |
Reaction Steps
A solution of 1-Chloro-2-nitro-4-((E)-2-nitro-propenyl)-benzene (13.6 g, 56 mmol) in glacial acetic acid (100 ml) is added slowly to a stirred slurry of Iron powder (34 g, 610 mmol) in glacial acetic acid (100 ml) at 60° C. The reaction mixture is stirred at 60° C. for 1 hour then allowed to cool to room temperature and stirred overnight. The reaction mixture is poured onto ice-water (300 ml) and filtered through Celite® (filter agent) washing with DCM (500 ml). The organic portion is separated and washed with water (2×300 ml) and brine (300 ml), dried over MgSO4, filtered and concentrated in vacuo to give a brown oil. The crude residue is absorbed onto silica and purification by flash chromatography on silica eluting with 20% EtOAc/Hexanes affords the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263585B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-98bfb31d7fc645f8916e5a652350f29c |
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| Source note | uspto-grants-2012_09 |
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