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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529666Generated: November 3, 2026

Urea → 2-Tert-butyl-5-nitrophenol

https://huagongshe.com/reaction/1529666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
Reactant2-Tert-butyl-5-nitroanilineHCID 826103—
ReactantSulfuric acid hydrate (1:1)HCID 21910475—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product2-Tert-butyl-5-nitrophenolHCID 2195961762%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a mixture of 2-tert-butyl-5-nitroaniline (1.94 g, 10 mmol) in 40 mL of 15% H2SO4 was added dropwise a solution of NaNO2 (763 mg, 11.0 mmol) in water (3 mL) at 0° C. The resulting mixture was stirred at 0-5° C. for 5 min. Excess NaNO2 was neutralized with urea, then 5 mL of H2SO4—H2O (v/v 1:2) was added and the mixture was refluxed for 5 min. Three additional 5 mL aliquots of H2SO4—H2O (v/v 1:2) were added while heating at reflux. The reaction mixture was cooled to room temperature and extracted with EtOAc twice. The combined organic layers were washed with brine and dried over MgSO4. After removal of solvent, the residue was purified by column chromatography (0-10% EtOAc-Hexane) to give 2-tert-butyl-5-nitrophenol (C-1-a) (1.2 g, 62%). 1H NMR (400 MHz, CDCl3) δ 7.76 (dd, J=8.6, 2.2 Hz, 1H), 7.58 (d, J=2.1 Hz, 1H), 7.43 (d, J=8.6 Hz, 1H), 5.41 (s, 1H), 1.45 (s, 9H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090619B2
Source datasetuspto-grants-2015_07
ORD IDord-a444ee8213924b3eadd262fc9ac19dd6
Source noteuspto-grants-2015_07