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2-Acetylpyrrole → (2E)-3-(Dimethylamino)-1-(1H-pyrrol-2-yl)-2-propen-1-one

HRID 2232296
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HRID 2232296 반응식
[C:1]([C:4]1[NH:5][CH:6]=[CH:7][CH:8]=1)(=[O:3])[CH3:2].C(O[CH:14](N(C)C)[N:15]([CH3:17])[CH3:16])(C)(C)C>CCCCCC>[CH3:14][N:15]([CH3:17])/[CH:16]=[CH:2]/[C:1]([C:4]1[NH:5][CH:6]=[CH:7][CH:8]=1)=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 140792-AcetylpyrroleHCID 79885tert-Butoxy bis(dimethylamino)methane

생성물 1

HCID 14346958(2E)-3-(Dimethylamino)-1-(1H-pyrrol-2-yl)-2-propen-1-one수율 42.1%

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

A mixture of 39.6 g of 2-acetylpyrrole and 104 ml (87.7 g) of tert-butoxy bis(dimethylamino)methane was heated on a steam bath for 20 minutes. The reaction was allowed to subside, then heating was continued for 6 hours. The mixture solidified then was slurried in hexane with chilling. The crude product was collected, washed with hexane and dried. The solid was dissolved in chloroform containing 5% methanol and filtered through magnesium silicate. The eluent was evaporated in vacuo and the residue was recrystallized from dichloromethane/hexane containing a small amount of methanol. The solid was collected, washed with hexane then dried in vacuo giving 25.1 g of the desired compound as yellow crystals, mp 192°-193° C. (dec.).

후처리

  1. temperaturewas heated on a steam bath for 20 minutes
  2. temperatureheating
  3. temperaturewith chilling
  4. customThe crude product was collected
  5. washwashed with hexane
  6. customdried
  7. dissolutionThe solid was dissolved in chloroform containing 5% methanol
  8. filtrationfiltered through magnesium silicate
  9. customThe eluent was evaporated in vacuo
  10. customthe residue was recrystallized from dichloromethane/hexane containing a small amount of methanol
  11. customThe solid was collected
  12. washwashed with hexane
  13. customthen dried in vacuo

출처 및 근거

ORD 기록
ord-ed57169f3e6744bfadceccb79579802d
출처 데이터셋
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04788195

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