HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745575Generated: October 25, 2026
Acetic Acid → 6-Nitro-1,3-benzodioxol-5-amine
https://huagongshe.com/reaction/745575
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-(6-Nitro-1,3-benzodioxol-5-yl)acetamide | HCID 540215 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Nitro-1,3-benzodioxol-5-amine | HCID 602665 | 95.1% |
Reaction Steps
40 g of 5-acetamino-6-nitro-1,3-benzodioxole were dissolved with heating in 4 l of methanol in a 10 l round flask equipped with a reflux condenser. To this hot solution was added a boiling solution of 40 g of sodium methoxide in 4 l of methanol and the mixture was boiled under reflux for exactly 15 minutes. Then, the reaction was interrupted by adding 220 ml of glacial acetic acid. The methanol was removed by distillation and the last traces thereof, together with the glacial acetic acid, were removed by a two-fold evaporation with toluene. The product went into solution with 3 l of methylene chloride and could be freed from the organic residues by suction filtration. The methylene chloride solution was filtered through silicon dioxide and evaporated in vacuo. The residue, recrystallized from isopropanol, gave 30.9 g (95% of theory) of 5-amino-6-nitro-1,3-benzodioxole of melting point 203°-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04599347 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-5db1c651cb40476093ba6515ba0ec03a |
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| Source note | uspto-grants-1986_07 |
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