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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115877Generated: October 29, 2026

Sulfuric Acid → 2-Tert-butyl-5-nitroaniline

https://huagongshe.com/reaction/2115877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium NitrateHCID 24434—
Reactant2-tert-ButylanilineHCID 80574—
Product2-Tert-butyl-5-nitroanilineHCID 826103—

Reaction Steps

Concentrated sulfuric acid (1 L) was cooled to −10° C. with a dry ice-isopropanol bath in a 2 L 3-necked round bottom flask fitted with a mechanical stirrer and temperature probe. The 2-t-butylaniline (109 g, 730 mmol) was added, giving a clumpy solid. Once the temperature of the mixture was stabilized at −10° C., the potassium nitrate (101 g, 1001 mmol) was added portion wise, as a solid, over a 4-hour period, maintaining the temperature between −20 and −5° C. Once all of the potassium nitrate was added, the reaction was left to stir overnight with gradual warming to RT. The reaction was quenched by diluting with water and then extracting three times with EtOAc. The EtOAc extracts were washed multiple times with saturated NaHCO3, until gas evolution ceased, then with brine. The EtOAc extracts were then combined, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure giving a black oil. The oil was eluted through a column of silica gel with EtOAc: hexanes gradient 5-50%. Solvent evaporation afforded 2-tert-butyl-5-nitrobenzenamine as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435823B2
Source datasetuspto-grants-2008_10
ORD IDord-29c7a18f59354b7caeb08759e0864fff
Source noteuspto-grants-2008_10