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HCID 59306518, 화합물 → Ethyl 3-cyano-2,4,5-trifluorobenzoate

HRID 2241118
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HRID 2241118 반응식
O[N:2]=[CH:3][C:4]1[C:5]([F:17])=[C:6]([CH:12]=[C:13]([F:16])[C:14]=1[F:15])[C:7]([O:9][CH2:10][CH3:11])=[O:8]>ClC(Cl)(Cl)C#N>[C:3]([C:4]1[C:5]([F:17])=[C:6]([CH:12]=[C:13]([F:16])[C:14]=1[F:15])[C:7]([O:9][CH2:10][CH3:11])=[O:8])#[N:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 59306518HCID 59306518, 화합물

생성물 1

HCID 18417534Ethyl 3-cyano-2,4,5-trifluorobenzoate

시약·촉매·용매 1

HCID 11011Trichloroacetonitrile용매

반응 조건

온도
90 °C

실험 절차

Ethyl 3-hydroxyiminomethyl-2,4,5-trifluorobenzoate (5.5 g, 24.0 mmol) was dissolved in trichloroacetonitrile (25 g), and the solution was stirred at 90° C. for 16 hours. The reaction mixture was left to cool, and the solid matter that precipitated was separated through filtration. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel chromatography (eluent; n-hexane ethyl acetate=10:1), to thereby yield the title compound as a colorless oily substance (3.35 g, 61%).

후처리

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  • waitThe reaction mixture was left
  • temperatureto cool
  • customthe solid matter that precipitated
  • customwas separated through filtration
  • concentrationThe filtrate was concentrated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-80b86f27b43745fbbfc18e864e2882f6
    출처 데이터셋
    uspto-grants-2010_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07723524B2

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