Urea → 2-Tert-butyl-5-nitrophenol

HRID 401301

반응식

HRID 401301 반응식
[C:1]([C:5]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][C:6]=1N)([CH3:4])([CH3:3])[CH3:2].N([O-])=[O:16].[Na+].NC(N)=O.OS(O)(=O)=O.O>OS(O)(=O)=O.O>[C:1]([C:5]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][C:6]=1[OH:16])([CH3:4])([CH3:3])[CH3:2]

참가 물질

7

반응 조건

온도
2.5 °C

실험 절차

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.

후처리

  1. temperaturethe mixture was refluxed for 5 min
  2. temperaturewhile heating
  3. temperatureat reflux
  4. temperatureThe reaction mixture was cooled to room temperature
  5. extractionextracted with EtOAc twice
  6. washThe combined organic layers were washed with brine
  7. dry with materialdried over MgSO4
  8. customAfter removal of solvent
  9. customthe residue was purified by column chromatography (0-10% EtOAc-Hexane)

출처 및 근거

ORD 기록
ord-6149daed63604e4e8b4ffc5776674110
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08741925B2

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