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Acetic-formic anhydride → N-(4,6-dimethylpyrimidin-2-yl)-formanilide

HRID 2231629
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반응식

HRID 2231629 반응식
[NH:1]([C:8]1[N:13]=[C:12]([CH3:14])[CH:11]=[C:10]([CH3:15])[N:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:16](OC=O)(=[O:18])C>>[CH3:14][C:12]1[CH:11]=[C:10]([CH3:15])[N:9]=[C:8]([N:1]([CH:16]=[O:18])[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[N:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 75269Acetic-formic anhydrideHCID 91650Pyrimethanil

생성물 1

HCID 14327563N-(4,6-dimethylpyrimidin-2-yl)-formanilide

실험 절차

2-Anilino-4,6-dimethylpyrimidine (10 g) was added to formic-acetic anhydride (prepared from formic acid (5 ml) and acetic anydride (12 ml)) and the mixture heated gently to 40° to give a clear solution. After standing for 4 days, a crystalline solid separated and toluene was added to give a clear solution again. The mixture was evaporated to dryness, more toluene added and reevaporated. The product was recrystallised from ethyl acetate/light petroleum to give N-(4,6-dimethylpyrimidin-2-yl)-formanilide, m.p. 134°-5°. (Compound 3).

후처리

  1. temperaturethe mixture heated gently to 40°
  2. customto give a clear solution
  3. customa crystalline solid separated
  4. additiontoluene was added
  5. customto give a clear solution again
  • customThe mixture was evaporated to dryness, more toluene
  • additionadded
  • customreevaporated
  • customThe product was recrystallised from ethyl acetate/light petroleum
  • 출처 및 근거

    ORD 기록
    ord-e3918f7c53824b01b596dc4d8f4dfbd6
    출처 데이터셋
    uspto-grants-1988_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04783459

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