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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73967생성일: 2026년 10월 25일

Urea → 2-Tert-butyl-5-nitrophenol

https://huagongshe.com/reaction/73967

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참여 물질

역할이름HCID투입량
반응물UreaHCID 1176—
반응물2-Tert-butyl-5-nitroanilineHCID 826103—
반응물Sulfuric acid hydrate (1:1)HCID 21910475—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
용매Sulfuric AcidHCID 1118—
생성물2-Tert-butyl-5-nitrophenolHCID 2195961762%

반응 조건

온도2.5 °C

반응 단계

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); HPLC ret. time 3.46 min, 10-99% CH3CN, 5 min run.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829204B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-a132ed9a78914d1eaa7166dee7046539
출처 메모uspto-grants-2014_09