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Dimethyl Sulfoxide → 2-(4-Fluorophenyl)-2-methylpropanal

HRID 885171
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HRID 885171 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[F:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([CH3:22])([CH3:21])[CH2:19][OH:20])=[CH:14][CH:13]=1.C(N(CC)CC)C>ClCCl.O>[F:11][C:12]1[CH:13]=[CH:14][C:15]([C:18]([CH3:22])([CH3:21])[CH:19]=[O:20])=[CH:16][CH:17]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 212628022-(4-Fluorophenyl)-2-methylpropan-1-ol

생성물 1

HCID 820747502-(4-Fluorophenyl)-2-methylpropanal

시약·촉매·용매 2

HCID 962Water용매
HCID 6344
Dichloromethane
용매
4회

반응 조건

온도
-60 °C

실험 절차

To a stirred solution of oxalyl chloride (2.81 ml) in dichoromethane (30 ml) at −60° C. was added dropwise a solution of dry dimethyl sulphoxide (4.84 ml) in dichloromethane (20 ml). The mixture was stirred for 15 min at −60° C. and then a solution of 2-(4-fluoro-phenyl)-2-methyl-propan-1-ol (4.59 g; CAS 703-10-6) in dichloromethane (20 ml) was added dropwise. The mixture was stirred at −60° C. for 2 hours and then triethylamine (18.9 ml) was added dropwise. The reaction mixture was allowed to warm to room temperature and diluted with water and with dichloromethane. The phases were separated and the organic phase was washed with water and then dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (SiO2, heptane/EtOAc gradient) to yield a colourless oil, (3.47 g, 77%).

후처리

  1. stirringThe mixture was stirred at −60° C. for 2 hours
  2. temperatureto warm to room temperature
  3. customThe phases were separated
  4. washthe organic phase was washed with water
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by column chromatography (SiO2, heptane/EtOAc gradient)
  8. customto yield a colourless oil, (3.47 g, 77%)

출처 및 근거

ORD 기록
ord-73e1d86c933d4f29b46211e79ac39a92
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08242153B2

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