Dimethylformamide → 1-cyclopropyl-1H-pyrrole-2-carbaldehyde

HRID 420137ノート

反応式

HRID 420137 の反応式
O=P(Cl)(Cl)Cl.[CH:6]1([N:9]2[CH:13]=[CH:12][CH:11]=[CH:10]2)[CH2:8][CH2:7]1.CN([CH:17]=[O:18])C>>[CH:6]1([N:9]2[CH:13]=[CH:12][CH:11]=[C:10]2[CH:17]=[O:18])[CH2:8][CH2:7]1

参加物

4

実験手順

44.46 ml of POCl3 was added to a stirred solution of 1-cyclopropyl-1H-pyrrole (46.46 g) in 37 ml of DMF with cooling with ice, then the mixture was stirred at room temperature overnight. The mixture was poured into 336 ml of 5N NaOHaq with cooling with ice, and the mixture was made basic with an additional 5N NaOHaq. The mixture was extracted with CH2Cl2 and the organic extract was dried over Na2SO4, concentrated, and the residue was purified on SiO2 column chromatography (n-hexane-EtOAc system) to give 38.91 g of 1-cyclopropyl-1H-pyrrol-2-carbaldehyde as a colorless oil.

後処理

  1. temperaturewith cooling with ice
  2. additionThe mixture was poured into 336 ml of 5N NaOHaq
  3. temperaturewith cooling with ice
  4. extractionThe mixture was extracted with CH2Cl2
  5. extractionthe organic extract
  6. dry with materialwas dried over Na2SO4
  7. concentrationconcentrated
  8. customthe residue was purified on SiO2 column chromatography (n-hexane-EtOAc system)

出典と根拠

ORDレコード
ord-86f6625a749f44029d6544488f31e585
出典データセット
uspto-grants-2012_01
特許番号
US08093389B2

反応ノート

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