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3-Oxo-3-phenylpropionanilide → 3-Deoxyviridicatin

HRID 2380327
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HRID 2380327 반응식
[C:1]([CH2:9][C:10]([NH:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:11])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>S(=O)(=O)(O)O.O>[C:2]1([C:1]2[C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[NH:12][C:10](=[O:11])[CH:9]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 703983-Oxo-3-phenylpropionanilide

생성물 1

HCID 3759123-Deoxyviridicatin

시약·촉매·용매 2

HCID 962Water용매HCID 1118Sulfuric Acid용매

실험 절차

Benzoylacetanilide (150 g) (prepared according to the method of Brown et al., J. Am. Chem. Soc., 79, 2919, (1957)) in concentrated sulphuric acid (76%) (130 cc) is heated for 4 hours at 100° C. The reaction mixture is slowly poured with stirring in distilled water (3150 cc). The precipitate obtained is filtered, washed with water and then with acetone, and dried at 40° C. under reduced pressure. The residue obtained is recrystallised in ethanol. (white solid; m.p.=268°-269° C.)

후처리

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
The reaction mixture is slowly poured
  • customThe precipitate obtained
  • filtrationis filtered
  • washwashed with water
  • dry with materialwith acetone, and dried at 40° C. under reduced pressure
  • customThe residue obtained
  • customis recrystallised in ethanol
  • 출처 및 근거

    ORD 기록
    ord-e30dd51f81844c29b3ea24c2216b37f3
    출처 데이터셋
    uspto-grants-1994_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05366982

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