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Allyl bromide → 1-[3-(Allyloxy)phenyl]ethanone

HRID 1244122
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HRID 1244122 반응식
[CH3:1][C:2]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]([OH:10])[CH:9]=1)=[O:3].C(=O)([O-])[O-].[K+].[K+].Br[CH2:18][CH:19]=[CH2:20]>CC(C)=O>[CH2:20]([O:10][C:8]1[CH:9]=[C:4]([C:2](=[O:3])[CH3:1])[CH:5]=[CH:6][CH:7]=1)[CH:19]=[CH2:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7841Allyl bromideHCID 84873-HydroxyacetophenoneHCID 11430Potassium Carbonate

생성물 1

HCID 2579581-[3-(Allyloxy)phenyl]ethanone

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To solution of 3-hydroxyacetophenone (2.140 g, 15.72 mmol) in acetone (100 mL) was added potassium carbonate (4.344 g, 31.43 mmol), and 3-bromo-propene (2.282 g, 18.86 mmol) and the reaction was stirred at room temperature for 16 h. The solvent was removed in vacuo and water (25 mL) was added to the reaction mixture and then extracted with ethyl acetate (3×60 mL). The organic extracts were washed with brine (15 mL), dried (Na2SO4) and concentrated to give the title compound which was used as is in the next step.

후처리

  1. customThe solvent was removed in vacuo and water (25 mL)
  2. additionwas added to the reaction mixture
  3. extractionextracted with ethyl acetate (3×60 mL)
  4. washThe organic extracts were washed with brine (15 mL)
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8d3c60a8585e4faca3a916616cb0bc63
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07119205B2

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