Sodium Iodide → N1-[5-Acetyl-3-(tert-butyl)-2-hydroxyphenyl]acetamide

HRID 1295996노트

반응식

HRID 1295996 반응식
Cl[Si](C)(C)C.[C:6]([C:9]1[CH:10]=[C:11]([C:23]([CH3:26])([CH3:25])[CH3:24])[C:12]([O:19]COC)=[C:13]([NH:15][C:16](=[O:18])[CH3:17])[CH:14]=1)(=[O:8])[CH3:7].[I-].[Na+].C(=O)([O-])O.[Na+]>O1CCCC1>[C:6]([C:9]1[CH:10]=[C:11]([C:23]([CH3:26])([CH3:25])[CH3:24])[C:12]([OH:19])=[C:13]([NH:15][C:16](=[O:18])[CH3:17])[CH:14]=1)(=[O:8])[CH3:7]

참가 물질

6

실험 절차

Chlorotrimethylsilane (36.5 ml, 288 mmol) was added dropwise to a solution of the N1-[5-acetyl-3-(tert-butyl)-2-(methoxymethoxy)phenyl]acetamide (56.2 g, 192 mmol) and sodium iodide (43.1 g, 288 mmol) in tetrahydrofuran (300 ml) under a nitrogen atmosphere while cooling on ice, and then the mixture was stirred at the same temperature for 10 minutes and at room temperature for 1 hour. The reaction mixture was poured into a saturated aqueous sodium hydrogencarbonate (400 ml)-ice (300 ml) mixed solvent while stirring. Following extraction twice with ethyl acetate, the organic layer was washed with saturated aqueous sodium hydrogencarbonate and brine in that order. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was recrystallized from ethyl acetate-n-hexane to yield the title compound (first crystallization=30.5 g, second crystallization=3.55 g, 71.3% yield) as white needle-like crystals.

후처리

  1. temperaturewhile cooling on ice
  2. additionmixed solvent
  3. stirringwhile stirring
  4. extractionextraction twice with ethyl acetate
  5. washthe organic layer was washed with saturated aqueous sodium hydrogencarbonate and brine in that order
  6. dry with materialAfter drying over anhydrous magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure
  8. customThe residue was recrystallized from ethyl acetate-n-hexane

출처 및 근거

ORD 기록
ord-0db4bfe286d94614994f42bdbbdb8fd7
출처 데이터셋
uspto-grants-2007_07
특허 번호
US07244730B2

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