Hexamethylenetetramine → 4-Isopropyl salicylaldehyde

HRID 229573ノート

反応式

HRID 229573 の反応式
[CH:1]([C:4]1[CH:5]=[C:6]([OH:10])[CH:7]=[CH:8][CH:9]=1)([CH3:3])[CH3:2].C1N2CN3CN(C2)CN1C3.FC(F)(F)[C:23](O)=[O:24]>>[OH:10][C:6]1[CH:5]=[C:4]([CH:1]([CH3:3])[CH3:2])[CH:9]=[CH:8][C:7]=1[CH:23]=[O:24]

参加物

4

反応条件

温度
60 °C

実験手順

To 100 mL of trifluoroacetic acid were added 25.39 g of 3-isopropylphenol and 26.14 g of hexamethylenetetramine. After being stirred at 60° C. for an hour, the reaction mixture was concentrated under reduced pressure. To the residue was added diluted hydrochloric acid, and the mixture was stirred at room temperature for 30 minutes. After the reaction mixture was extracted with ethyl acetate, the organic layer was washed with saturated aqueous sodium bicarbonate solution, and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: ethyl acetate-hexane) to give 6.69 g of 2-hydroxy-4-isopropylbenzaldehyde.

後処理

  1. concentrationthe reaction mixture was concentrated under reduced pressure
  2. additionTo the residue was added diluted hydrochloric acid
  3. stirringthe mixture was stirred at room temperature for 30 minutes
  4. extractionAfter the reaction mixture was extracted with ethyl acetate
  5. washthe organic layer was washed with saturated aqueous sodium bicarbonate solution, and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe solvent was removed under reduced pressure
  8. customthe residue was purified by column chromatography on silica gel (eluent: ethyl acetate-hexane)

出典と根拠

ORDレコード
ord-13b2b285557b44898d86e19d4d179eb5
出典データセット
uspto-grants-2009_07
特許番号
US07563822B2

反応ノート

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