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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181932Generated: November 2, 2026

Nitric Acid → Nitric Acid

https://huagongshe.com/reaction/1181932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactant2-Bromo-4-tert-butyl-1-methoxybenzeneHCID 12657723—
SolventAcetic AnhydrideHCID 7918—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductNitric AcidHCID 94470%
Product1-Bromo-5-(tert-butyl)-2-methoxy-3-nitrobenzeneHCID 5755002437%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromo-4-tert-butylanisole (4.54 g, 18.67 mmol) was dissolved in acetic anhydride (15 mL) and the solution was cooled to 0° C. A solution of nitric acid (70%, 2.5 mL) in acetic anhydride (2.5 mL) was prepared by the dropwise addition of HNO3 (70%, 2.5 mL) to Ac2O at 0° C. The HNO3 solution was pre-cooled to 0° C., and added dropwise to the stirred solution of the 2-bromo-4-tert-butylanisole over 5 min. The mixture was stirred at 0° C. for 1 h, then allowed to warm to room temperature and stirred overnight. The reaction mixture was diluted with EtOAc (150 mL) and saturated NaHCO3 (50 mL) This mixture was then neutralized by gradual addition of solid NaHCO3 until the pH was between 7-8. The organic layer was separated, washed with brine (50 mL) and dried over anhydrous Na2SO4. The solvents were removed in vacuo, the residue was purified by column chromatography (eluting with 3:1 hexane-EtOAc) to give 2-bromo-4-tert-butyl-6-nitroanisole (2 g, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285545B2
Source datasetuspto-grants-2007_10
ORD IDord-3cb8c80bd2a848f2b024a7b46b3f605b
Source noteuspto-grants-2007_10