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2-Propanone, 1-bromo-3-(4-nitrophenyl)- → HCID 13093759, 화합물

HRID 2412467
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HRID 2412467 반응식
Br[CH2:2][C:3]([CH2:5][C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][CH:7]=1)=[O:4].[C:15]1(=[O:25])[NH:19][C:18](=[O:20])[C:17]2=[CH:21][CH:22]=[CH:23][CH:24]=[C:16]12.[K]>C1(C)C=CC=CC=1>[C:15]1(=[O:25])[N:19]([CH2:2][C:3]([CH2:5][C:6]2[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][CH:7]=2)=[O:4])[C:18](=[O:20])[C:17]2=[CH:21][CH:22]=[CH:23][CH:24]=[C:16]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 122323022-Propanone, 1-bromo-3-(4-nitrophenyl)-HCID 24194345Phthalimide potassium salt

생성물 1

HCID 13093759HCID 13093759, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 1-bromo-3-(4-nitrophenyl)acetone and potassium phthalimide (7.2 g.) in toluene (100 ml.) was heated under reflux with stirring for 4 hours. The mixture was filtered, the filtrate evaporated. The residue was purified by chromatography on silica gel using CH2Cl2 as eluant to give 1-phthalimido-3-(4-nitrophenyl)acetone, m.p. 184°.

후처리

temperature
was heated
  • temperatureunder reflux
  • filtrationThe mixture was filtered
  • customthe filtrate evaporated
  • customThe residue was purified by chromatography on silica gel
  • 출처 및 근거

    ORD 기록
    ord-c47d263c92f646cfbea3b935dec90581
    출처 데이터셋
    uspto-grants-1985_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04492692

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