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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
Reactant2-Bromo-4-(tert-butyl)anilineHCID 238591—
SolventSulfuric AcidHCID 1118—
Product2-Bromo-4-tert-butyl-5-nitroanilineHCID 5748269678%

Reaction Conditions

Temperature-7.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-5bb0af57423e422aba3b9283d59ab396
Source noteuspto-grants-2013_12