Water → Thymol

HRID 1915452노트

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HRID 1915452 반응식
[CH:1]([C:4]1[CH:10]=[CH:9][C:8]([N+]([O-])=O)=[CH:7][C:5]=1N)([CH3:3])[CH3:2].OS(O)(=O)=O.N([O-])=O.[Na+].N[C:24](N)=O.[OH2:27]>>[CH:1]([C:4]1[CH:10]=[CH:9][C:8]([CH3:24])=[CH:7][C:5]=1[OH:27])([CH3:3])[CH3:2]

참가 물질

6

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온도
0 °C

실험 절차

2-Isopropyl-5-nitro-aniline (1.89 g, 10.49 mmol) was added dropwise to a mixture of conc. H2SO4 (9 mL) and H2O (50 mL). This reaction mixture was cooled to 0° C. and a solution of NaNO2 (763 mg, 11.06 mmol) in H2O (2 mL) was added. The reaction mixture was stirred for 10 minutes and then 1 g of urea was added to decompose the excess NaNO2, followed by the addition of 10 mL of 1:2 conc. H2SO4: H2O. The reaction mixture was then refluxed for 10 minutes, cooled to room temperature and extracted with EtOAc, washed with brine, dried over MgSO4, filtered and concentrated. The residue was then purified via silica gel column chromatography using 10 to 20% EtOAc in hexanes to obtain 2-isopropyl-5-methyl-phenol (1.41 g, 89%). 1H NMR (400 MHz, CDCl3) δ 7.79 (dd, J=8.5, 2.3 Hz, 1H), 7.63 (d, J=2.3 Hz, 1H), 7.33 (d, J=8.5 Hz, 1H), 7.26 (s, 1H), 3.39-3.18 (m, 1H), 1.29-1.26 (m, 6H).

후처리

  1. temperatureThe reaction mixture was then refluxed for 10 minutes
  2. temperaturecooled to room temperature
  3. extractionextracted with EtOAc
  4. washwashed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was then purified via silica gel column chromatography

출처 및 근거

ORD 기록
ord-47716b7ca31a49e0a90336d20bb13ed1
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08614327B2

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