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Dichromate ion → 1-(5-Bromo-2-fluorophenyl)ethanone

HRID 899406
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HRID 899406 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:11])=[C:6]([CH:8]([OH:10])[CH3:9])[CH:7]=1.[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O>ClCCl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:11])=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24503Dichromate ionHCID 441820551-(5-Bromo-2-fluorophenyl)ethanol

생성물 1

HCID 226074761-(5-Bromo-2-fluorophenyl)ethanone수율 84.9%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
20 °C

실험 절차

Compound 4b (50.0g, 228 mmol) along with 300 ml dichloromethane was charged into 2 liter round bottom flask. Crushed pyridinum dichromate (171.0 g, 456 mmol) and powdered molecular sieves (10 g) were both added into the flask. The heterogeneous reaction mixture was stirred for 16 hours at 20° C. The resulting reaction mixture was filtered through celite and washed with ether (500 ml×3). The combined filtrate was concentrated under reduced pressure. The crude product was eluted through a short silica gel pad (3 inches in length) withlo% EtOAc in hexane. The resulting product (42.0 g, yield=84%) was used for the following step.

후처리

  1. additionboth added into the flask
  2. customThe resulting reaction mixture
  3. filtrationwas filtered through celite
  4. washwashed with ether (500 ml×3)
  5. concentrationThe combined filtrate was concentrated under reduced pressure
  6. washThe crude product was eluted through a short silica gel pad (3 inches in length) withlo% EtOAc in hexane

출처 및 근거

ORD 기록
ord-b394b9f98be64a318a94025855d987d9
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07354944B2

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