Sulfuric Acid → 7-Isopropyl-2,4-dimethyl-benzooxazol-6-ol

HRID 38443

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HRID 38443 반응식
[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([OH:9])=[C:4]([CH:10]([CH3:12])[CH3:11])[C:3]=1[OH:13].O[C:15]1C=C(C(C)C)C=C(O)[C:20]=1C.C1(C)CC(=O)C(C(C)C)C(=O)C1.C(OC(OCC)OCC)C.OS(O)(=O)=O>CO.[Cl-].[Ti+4].[Cl-].[Cl-].[Cl-]>[CH:10]([C:4]1[C:3]2[O:13][C:15]([CH3:20])=[N:1][C:2]=2[C:7]([CH3:8])=[CH:6][C:5]=1[OH:9])([CH3:11])[CH3:12]

참가 물질

8

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온도
0 °C

실험 절차

To a flask charged with 4-amino-2-isopropyl-5-methyl-benzene-1,3-diol (250 mg, 1.4 mmol) (Treibs and Albrecht, “The dihydroxycymenes. IV. Isocymorcin (3,5-dihydroxycymene) from 3,5-menthanedione by dehydrogenation and total synthesis,” Journal fuer Praktische Chemie (1961), 13, 291-305), purged with argon, and cooled to 0° C., was sequentially added triethylorthoformate (0.53 mL, 4.2 mmol), MeOH (2.5 mL), and a 10% v/v solution of H2SO4 in MeOH (25 μL). The reaction was allowed to warm to room temperature slowly, stirred overnight, quenched with saturated NaHCO3, and concentrated. The residue was partitioned between water and methylene chloride. The combined organic phases were dried with Na2SO4 and concentrated. Purification via flash chromatography afforded 175 mg of 7-isopropyl-2,4-dimethyl-benzooxazol-6-ol.

후처리

  1. custompurged with argon
  2. temperatureto warm to room temperature slowly
  3. customquenched with saturated NaHCO3
  4. concentrationconcentrated
  5. customThe residue was partitioned between water and methylene chloride
  6. dry with materialThe combined organic phases were dried with Na2SO4
  7. concentrationconcentrated
  8. customPurification via flash chromatography

출처 및 근거

ORD 기록
ord-f48841bbb421402992e308f5406e6763
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08524725B2

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