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Benzyl Chloride → 3,4-Diphenylbutan-2-one

HRID 1076328
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반응식

HRID 1076328 반응식
[H-].[Na+].[C:3]1([CH2:9][C:10](=[O:12])[CH3:11])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:13](Cl)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C(COC)OC>[C:3]1([CH:9]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:10](=[O:12])[CH3:11])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7503Benzyl ChlorideHCID 7678PhenylacetoneHCID 24758Sodium hydride

생성물 1

HCID 2488503,4-Diphenylbutan-2-one

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매3회

실험 절차

Sodium hydride (8.4 g., 0.2 mole, oil dispersion) is suspended in glyme (400 ml.) and phenyl acetone (26.8 g., 0.2 mole) in glyme (50 ml.) is added dropwise with stirring. After complete addition the mixture is heated to reflux for one hour then cooled in a cold water bath. A solution of benzyl chloride (25.3 g., 0.2 mole) in glyme (50 ml.) is added then the mixture is refluxed for 12 hours. Removal of the inorganic salts by filtration followed by vacuum distillation of the residue gives 31.06 g., b.p 104°-107°/0.1 mm

후처리

  1. additionAfter complete addition the mixture
  2. temperatureis heated
  3. temperatureto reflux for one hour
  4. temperaturethen cooled in a cold water bath
  5. temperaturethe mixture is refluxed for 12 hours
  6. customRemoval of the inorganic salts
  7. filtrationby filtration
  8. distillationfollowed by vacuum distillation of the residue
  9. customgives 31.06 g
  10. customb.p 104°-107°/0.1 mm

출처 및 근거

ORD 기록
ord-32565c39c3654156ad749da8d6274fb3
출처 데이터셋
uspto-grants-1976_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03956374

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