tert-Butanol → (2,6-Difluoro-3,5-dimethoxy-phenyl)-carbamic Acid Tert-Butyl Ester

HRID 459944노트

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HRID 459944 반응식
[F:1][C:2]1[C:10]([O:11][CH3:12])=[CH:9][C:8]([O:13][CH3:14])=[C:7]([F:15])[C:3]=1C(O)=O.C([N:18]([CH2:21]C)CC)C.[C:23]([OH:27])([CH3:26])([CH3:25])[CH3:24].C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:35])C=CC=CC=1>C1(C)C=CC=CC=1>[C:23]([O:27][C:21](=[O:35])[NH:18][C:3]1[C:7]([F:15])=[C:8]([O:13][CH3:14])[CH:9]=[C:10]([O:11][CH3:12])[C:2]=1[F:1])([CH3:26])([CH3:25])[CH3:24]

참가 물질

6

실험 절차

To a stirred mixture of 47.7 g (0.22 mol) of 2,6-difluoro-3,5-dimethoxy benzoic acid, 32 mL (0.22 mol) of triethylamine and 16.2 g (0.22 mol) of t-butanol in 500 mL of toluene, 48.2 mL (0.22 mol) of diphenylphosphoryl azide was added in one portion and the mixture was heated to 60° C.–70° C. After approximately 1 hour, the reaction was completed and the mixture was cooled down. The toluene was removed in vacuo. Then, ethyl acetate was added and the resulting solution was washed two times with saturated potassium hydrogen-phosphate solution, two times with saturated sodium bicarbonate solution, one time with brine, dried over sodium sulfate, filtered and evaporated. The crude product was purified by column chromatography: 1 kg of silica eluting with dichloromethane to give 45 g (71%) of the title compound.

후처리

  1. additionwas added in one portion
  2. temperaturethe mixture was heated to 60° C.–70° C
  3. temperaturethe mixture was cooled down
  4. customThe toluene was removed in vacuo
  5. additionThen, ethyl acetate was added
  6. washthe resulting solution was washed two times with saturated potassium hydrogen-phosphate solution, two times with saturated sodium bicarbonate solution, one time with brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. customevaporated
  10. customThe crude product was purified by column chromatography

출처 및 근거

ORD 기록
ord-13e8387af2ac4144bd81fb285a1d161d
출처 데이터셋
uspto-grants-2007_03
특허 번호
US07196090B2

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