反応 #54955

ord-040e02245ccf4febaf7f5fc948a20887

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出the mixture was extracted with chloroform (4×70 ml)
  2. 2
    抽出The combined chloroform phases were extracted with saturated sodium bicarbonate solution (4×30 ml)
  3. 3
    洗浄washed with chloroform (100 ml)
  4. 4
    抽出The precipitated product was extracted with chloroform (3×100 ml)
  5. 5
    乾燥the combined extracts dried over magnesium sulphate
  6. 6
    その他After removing solvent
  7. 7
    その他the product was recrystallised from benzene/hexane (1;1)

実験手順

2-(2-Ethyl-4-oxo-4H-1-benzopyran-6-yl)propan-1-ol (3.0 g; 0.0129 mol) was dissolved in acetone (20 ml) and Jones Reagent (Example 2) was slowly added until the solution attained a permanent brown colour. Water (100 ml) was added and the mixture was extracted with chloroform (4×70 ml). The combined chloroform phases were extracted with saturated sodium bicarbonate solution (4×30 ml). The aqueous phases were combined, washed with chloroform (100 ml) and then acidified with concentrated hydrochloric acid. The precipitated product was extracted with chloroform (3×100 ml) and the combined extracts dried over magnesium sulphate. After removing solvent, the product was recrystallised from benzene/hexane (1;1) to yield a pale yellow amorphous solid (1.4 g) mp 128°-128.5°.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04151179uspto-grants-1979_04