(6-Iodopyridin-3-yl)methanol → 6-Iodopyridine-3-carbaldehyde

HRID 1864572ノート

反応式

HRID 1864572 の反応式
[I:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][OH:9])=[CH:4][CH:3]=1>ClCCl.[O-2].[O-2].[Mn+4]>[I:1][C:2]1[N:7]=[CH:6][C:5]([CH:8]=[O:9])=[CH:4][CH:3]=1

参加物

4

実験手順

63 g (723 mmol) of manganese dioxide are added to a solution of 17 g (72 mmol) of (6-iodopyrid-3-yl)methanol in 600 ml of dichloromethane. The reaction medium is stirred at room temperature for 20 hours and then filtered through Celite. The precipitate is washed thoroughly with water and the filtrate is evaporated under vacuum. The residue obtained is taken up in dichloromethane and the insoluble material is again filtered off. After evaporation of the filtrate, 13.2 g (78%) of 6-iodopyridine-3-carbaldehyde are obtained in the form of a pale yellow solid with a melting point of 141° C.

後処理

  1. filtrationfiltered through Celite
  2. washThe precipitate is washed thoroughly with water
  3. customthe filtrate is evaporated under vacuum
  4. customThe residue obtained
  5. filtrationthe insoluble material is again filtered off
  6. customAfter evaporation of the filtrate, 13.2 g (78%) of 6-iodopyridine-3-carbaldehyde
  7. customare obtained in the form of a pale yellow solid with a melting point of 141° C.

出典と根拠

ORDレコード
ord-fcd6b61a62354943b0685c981a0713b1
出典データセット
uspto-grants-2009_12
特許番号
US07625914B2

反応ノート

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