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Water → HCID 20246850, 화합물

HRID 1589357
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HRID 1589357 반응식
Br[C:2]1([C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=2)[C:10](=[O:11])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[C:3]1=[O:18].[OH2:26]>[N+]([O-])([O-])=O.[Ag+]>[Cl:25][C:22]1[CH:21]=[CH:20][C:19]([C:2]2([OH:26])[C:10](=[O:11])[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][C:8]=3[C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)[C:3]2=[O:18])=[CH:24][CH:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 962WaterHCID 20246842HCID 20246842, 화합물

생성물 1

HCID 20246850HCID 20246850, 화합물

시약·촉매·용매 1

HCID 24470Silver Nitrate촉매

실험 절차

A mixture of 2-bromo-2-(p-chlorophenyl)-4-phenylindane-1,3-dione (0.3 g), silver nitrate (0.15 g) ethanol (3 ml) and water (3 ml) was heated under reflux for 2 hours. After cooling, the precipitated solid was filtered off. The solvent was removed from the filtrate under reduced pressure and the residual solid was chromatographed in silica. Recrystallisation from ethanol-water of the fraction eluted with ethyl acetate afforded 2-(p-chlorophenyl)-2-hydroxy-4-phenylindane-1,3-dione, m.p. 161-163.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 2 hours
  3. temperatureAfter cooling
  4. filtrationthe precipitated solid was filtered off
  5. customThe solvent was removed from the filtrate under reduced pressure
  6. customthe residual solid was chromatographed in silica
  7. customRecrystallisation from ethanol-water of the fraction
  8. washeluted with ethyl acetate

출처 및 근거

ORD 기록
ord-24eefafd273e41a59ea8ebedf4409b9f
출처 데이터셋
uspto-grants-1986_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04569945

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