Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251845Generated: November 1, 2026

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

https://huagongshe.com/reaction/2251845

Reaction equation

Participants

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

Reaction Steps

Concentrated H2SO4 (1 L) was cooled to −10° C. with a dry ice-iPrOH bath in a 2 L 3-neck round bottom flask fitted with a mechanical stirrer and temperature probe. 2-t-Butylaniline (109 g, 730 mmol) was added, giving a clumpy solid. Once the temperature of the mixture was stabilized at −10° C., KNO3 (101 g, 1001 mmol) was added portion wise, as the solid, over 4 h, maintaining the temperature between −20 and −5° C. Once all of the KNO3 was added, the reaction was stirred overnight with gradual warming to RT. The reaction was quenched by diluting with water then extracted with EtOAc (3×). The EtOAc extracts were washed multiple times with saturated NaHCO3(aq), until gas evolution ceased, then with brine. The EtOAc extracts were combined, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure giving a black oil. The oil was eluted through a 36×7 cm column of silica gel with a 5%; 10%; 15%; 25%; and 50% EtOAc:Hexanes step gradient (2 L each step) giving a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320992B2
Source datasetuspto-grants-2008_01
ORD IDord-a44c2053cb114b3f92ada0dc0e141828
Source noteuspto-grants-2008_01