HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908583Generated: October 27, 2026
Potassium Nitrate → 2-Bromo-4-tert-butyl-5-nitroaniline
https://huagongshe.com/reaction/1908583
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 2-Bromo-4-(tert-butyl)aniline | HCID 238591 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 2-Bromo-4-tert-butyl-5-nitroaniline | HCID 57482696 | 78% |
Reaction Steps
2-Bromo-4-tert-butyl-phenylamine (160 g, 0.71 mol) was added dropwise to H2SO4 (410 mL) at room temperature to yield a clear solution. This clear solution was then cooled down to −5 to −10° C. A solution of KNO3 (83 g, 0.82 mol) in H2SO4 (410 mL) was added dropwise while the temperature was maintained between −5 to −10° C. Upon completion, the reaction mixture was poured into ice/water and extracted with EtOAc. The combined organic layers were washed with 5% Na2CO3 and brine, dried over Na2SO4 and concentrated. The residue was purified by a column chromatography (ethyl acetate/petroleum ether 1:10) to give 2-bromo-4-tert-butyl-5-nitro-phenylamine as a yellow solid (150 g, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598181B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-5bb0af57423e422aba3b9283d59ab396 |
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| Source note | uspto-grants-2013_12 |
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