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Methanol → 2',3'-Dihydroxyacetophenone

HRID 1603922
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HRID 1603922 반응식
C[O:2][C:3]1[C:8]([O:9]C)=[CH:7][CH:6]=[CH:5][C:4]=1[C:11](=[O:13])[CH3:12].B(Br)(Br)Br.CO>ClCCl>[OH:2][C:3]1[C:8]([OH:9])=[CH:7][CH:6]=[CH:5][C:4]=1[C:11](=[O:13])[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 25134Boron tribromideHCID 124074131-(2,3-Dimethoxyphenyl)ethan-1-one

생성물 1

HCID 64291102',3'-Dihydroxyacetophenone수율 76%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 2',3'-dimethoxyacetophenone (4.85 g, 26.9 mmol) in dichloromethane (100 ml) was added at -70° C. with a 1M boron tribromide solution in dichloromethane (68 ml). The mixture was left to cool, keeping stirring for 2.5 hours at room temperature, then added with methanol (70 ml), left under stirring for 1 h, thereafter evaporated to dryness. The residue was dissolved in ethyl acetate (250 ml), washed with 2% NaHCO3 (1×30 ml), dried and the solvent was evaporated off, to obtain a crude which was purified by crystallization in methanol, thereby obtaining 3.10 g of the title compound as a yellow solid (76% yield).

후처리

  1. waitThe mixture was left
  2. temperatureto cool
  3. waitleft
  4. stirringunder stirring for 1 h
  5. customevaporated to dryness
  6. dissolutionThe residue was dissolved in ethyl acetate (250 ml)
  7. washwashed with 2% NaHCO3 (1×30 ml)
  8. customdried
  9. customthe solvent was evaporated off
  10. customto obtain a crude which
  11. customwas purified by crystallization in methanol

출처 및 근거

ORD 기록
ord-2a1aa87c93d743f9a362f54196019a30
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05990142

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