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Chloroacetone → HCID 18317334, 화합물

HRID 1700463
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HRID 1700463 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[CH:9]1[CH2:14][C:13](=[O:15])[CH2:12][C:11](=[O:16])[CH2:10]1.[H-].[Na+].Cl[CH2:20][C:21](=O)[CH3:22]>CN(C=O)C>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[CH:9]1[CH2:14][C:13](=[O:15])[C:12]2[C:21]([CH3:22])=[CH:20][O:16][C:11]=2[CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6571ChloroacetoneHCID 24758Sodium hydrideHCID 183177375-(2,5-Dimethylphenyl)-1,3-cyclohexanedione

생성물 1

HCID 18317334HCID 18317334, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 5-(2,5-dimethylphenyl)cyclohexane-1,3-dione (mp194-195° C.; 1.08 g) in DMF (20 ml) was added 60% sodium hydride (0.22 g), and the mixture was stirred, under argon atmosphere, at room temperature for 15 minutes. To the mixture was added chloroacetone (0.45 ml), and the mixture was stirred at 150° C. overnight (16 hours). The reaction solution was cooled, and to the mixture was added ice-water. The mixture was extracted with ethyl acetate. The upper layer was washed with saturated brine, dried (anhydrous magnesium sulfate), and concentrated under reduced pressure, and the residue was subjected to silica gel chromatography and eluted with ethyl acetate/hexane to give 6-(2,5-dimethylphenyl)-3-methyl-4,5,6,7-tetrahydrobenzofuran-4-one (0.36 g).

후처리

  1. stirringthe mixture was stirred at 150° C. overnight (16 hours)
  2. temperatureThe reaction solution was cooled
  3. extractionThe mixture was extracted with ethyl acetate
  4. washThe upper layer was washed with saturated brine
  5. dry with materialdried (anhydrous magnesium sulfate)
  6. concentrationconcentrated under reduced pressure
  7. washeluted with ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-6e32494256884c179abf6356f66e9fb9
출처 데이터셋
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06350749B1

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