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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508321Generated: October 24, 2026

Water → 2-Bromo-4-(tert-butyl)-6-nitroaniline

https://huagongshe.com/en/reaction/508321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium SulfiteHCID 24437—
Reactant4-tert-Butyl-2-nitroanilineHCID 80573—
ReactantPyridinium hydrobromideHCID 21226041—
SolventAcetic AcidHCID 176—
Product2-Bromo-4-(tert-butyl)-6-nitroanilineHCID 5099785694%

Reaction Steps

A suspension of 4-tert-butyl-2-nitroaniline (1.033 g, 5.32 mmol) in glacial acetic acid (7.8 mL) was warmed with a heat gun until all solids had dissolved. The solution was then cooled and treated portion wise with pyridinium hydrobromide perbromide (1.96 g, 6.12 mmol). After addition, the solution was stirred at room temperature for 1 h. The mixture was added to water (50 mL) and treated with a small amount of sodium sulfite. After stirring for 30 min, the precipitate was collected by filtration. The solid obtained was washed with water and dissolved in EtOAc. Washed with water and brine. Dried over Na2SO4, filtered and concentrated under vacuum to provide the title compound as a yellow-orange solid (1.36 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095590B2
Source datasetuspto-grants-2015_08
ORD IDord-2cbc1eeeca104231a92bd89be3d30091
Source noteuspto-grants-2015_08