HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577612Generated: October 25, 2026
5,6-Dinitro-1,3-benzodioxole → 6-Nitro-1,3-benzodioxol-5-amine
https://huagongshe.com/reaction/577612
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5,6-Dinitro-1,3-benzodioxole | HCID 611325 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Nitro-1,3-benzodioxol-5-amine | HCID 602665 | 84.4% |
Reaction Steps
Compound 5,6-dinitrobenzo[d][1,3]dioxole (6.0 g, 28.3 mmol) was added to stirred glacial acetic acid (120 mL) under N2 atmosphere. After the mixture was heated to boiling, the heat source was removed and iron powder (4.75 g) added with vigorous stirring. Quick spontaneous boiling occurred, the mixture turned dark and the exothermic reaction subsided (2-5 min). The mixture was refluxed for 10 min and poured into ice/water. The orange-red product was isolated by filtration, dissolved in glacial acetic acid, and the solution filtered while hot. The filtrate was poured into ice-cold water. The orange-red solid product was isolated by filtration and dried to provide compound 6-nitrobenzo[d][1,3]dioxol-5-amine (4.35 g, 84%). LCMS: 183 [M+1]+; 1H NMR (DMSO-d6) δ 6.06 (s, 2H), 6.51 (s, 1H), 7.36 (s, 1H), 7.73 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040556B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-6e6029a8c7c24decb7ed0e385748c29e |
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| Source note | uspto-grants-2015_05 |
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