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Benzyl Bromide → HCID 18414640, 화합물

HRID 991587
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HRID 991587 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([CH2:9][CH2:10][CH3:11])[CH:3]=1.[CH2:12](Br)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[C:4]([CH2:9][CH2:10][CH3:11])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 221345104-Bromo-2-propylphenol

생성물 1

HCID 18414640HCID 18414640, 화합물수율 69.7%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a 100 ml acetone solution of 4-bromo-2-propylphenol 5.4 g (25.1 mol) and benzyl bromide 5.6 g (32.7 mmol) was added potassium carbonate 5.2 g (37.6 mmol). Resulting suspension was stirred under reflux temperature for overnight. Acetone was removed under reduced pressure, diluted with ethyl acetate and water. Organic phase was separated. Aqueous phase was extracted with ethyl acetate twice. The combined organic phases were dried over anhydrous sodium sulfate, filtered, concentrated, chromatographed on silica gel (hexanes: t-butyl methyl ether) to give 6.96 g of benzyl 4-bromo-2-propylphenyl ether as colorless oil.

후처리

  1. customResulting suspension
  2. temperatureunder reflux temperature for overnight
  3. customAcetone was removed under reduced pressure
  4. additiondiluted with ethyl acetate and water
  5. customOrganic phase was separated
  6. extractionAqueous phase was extracted with ethyl acetate twice
  7. dry with materialThe combined organic phases were dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customchromatographed on silica gel (hexanes: t-butyl methyl ether)

출처 및 근거

ORD 기록
ord-823dea59bfe942c895ccd52a42cd59a8
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06465497B2

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