Bromide ion → 1-[3-Tert-butyl-5-(3-hydroxy-2,2-dimethylpropoxy)-4-methoxyphenyl]ethanone

HRID 1524567노트

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HRID 1524567 반응식
[C:1]([C:5]1[CH:6]=[C:7]([C:14](=[O:16])[CH3:15])[CH:8]=[C:9]([OH:13])[C:10]=1[O:11][CH3:12])([CH3:4])([CH3:3])[CH3:2].C([O:20][CH2:21][C:22]([CH3:26])([CH3:25])[CH2:23]Br)(=O)C.C(=O)([O-])[O-].[Cs+].[Cs+].[Br-]>CN(C=O)C>[C:1]([C:5]1[CH:6]=[C:7]([C:14](=[O:16])[CH3:15])[CH:8]=[C:9]([O:13][CH2:23][C:22]([CH3:26])([CH3:25])[CH2:21][OH:20])[C:10]=1[O:11][CH3:12])([CH3:4])([CH3:2])[CH3:3]

참가 물질

6

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온도
150 °C

실험 절차

1-(3-tert-Butyl-5-hydroxy-4-methoxyphenyl)ethanone (O3.070; 2.00 g) and 3-bromo-2,2-dimethylpropyl acetate (2.54 g) were dissolved in DMF (15 ml), and cesium carbonate (3.69 g) was added. After stirring at 150° C. and max. 15 bar in a microwave for 2.5 h, a further 0.5 eq. of the bromide was added and the mixture was placed into the microwave at 150° C. for a further 2 h. Then the mixture was concentrated by rotary evaporation and the residue was partitioned between DCM and water. The DCM phase was removed, dried over magnesium sulfate, filtered and concentrated. The residue was purified using silica gel (120 g cartridge, n-heptane/MtB ether gradient of 0-50% within 60 min). 1.17 g of the title compound were obtained.

후처리

  1. waitthe mixture was placed into the microwave at 150° C. for a further 2 h
  2. concentrationThen the mixture was concentrated by rotary evaporation
  3. customthe residue was partitioned between DCM and water
  4. customThe DCM phase was removed
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified
  9. customsilica gel (120 g cartridge, n-heptane/MtB ether gradient of 0-50% within 60 min)

출처 및 근거

ORD 기록
ord-87260c9397574af2be29605d307bea42
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09079906B2

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