Tetrahydrofuran → HCID 13620271、化合物

HRID 1052239ノート

反応式

HRID 1052239 の反応式
[CH3:1][C:2](=[O:7])[CH2:3][C:4](=O)[CH3:5].COC(OC)[N:11]([CH3:13])C.O1CCCC1.Cl.Cl.[CH2:23]([NH:30]N)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>O.C(OCC)(=O)C>[CH2:23]([N:30]1[C:4]([CH3:5])=[C:3]([C:2](=[O:7])[CH3:1])[CH:13]=[N:11]1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

参加物

7

反応条件

温度
80 °C

実験手順

A mixture of pentane-2,4-dione (10.01 g) and 1,1-dimethoxy-N,N-dimethylmethanamine (12.51 g) was stirred at 80° C. for 1 hr. Tetrahydrofuran (20 mL) was added to the reaction mixture, benzylhydrazine dihydrochloride (21.46 g) was added by small portions under ice-cooling, and the mixture was stirred at 60° C. for 30 min. The reaction mixture was allowed to cool to room temperature, ethyl acetate (100 mL) and water (100 mL) were added, and the separated aqueous layer was extracted with ethyl acetate (50 mL×2). The combined organic layers were washed with brine (20 mL) and dried over anhydrous magnesium sulfate. Insoluble material was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (13.53 g) as a colorless oil.

後処理

  1. additionwas added by small portions under ice-
  2. temperaturecooling
  3. stirringthe mixture was stirred at 60° C. for 30 min
  4. temperatureto cool to room temperature
  5. extractionthe separated aqueous layer was extracted with ethyl acetate (50 mL×2)
  6. washThe combined organic layers were washed with brine (20 mL)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customInsoluble material was removed by filtration
  9. concentrationthe filtrate was concentrated under reduced pressure
  10. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

出典と根拠

ORDレコード
ord-141bf48a69ee48e5b11767b78a4a6710
出典データセット
uspto-grants-2016_07
特許番号
US09388195B2

反応ノート

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