Sulfuric Acid → Spiro(4.5)dec-6-ene-8-one

HRID 1478150

反応式

HRID 1478150 の反応式
[CH:1]1([CH:6]=O)[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:8]([C:10]([CH3:12])=[O:11])=[CH2:9].OS(O)(=O)=O.C([O-])(O)=O.[Na+]>C1(C)C=CC=CC=1>[CH2:2]1[C:1]2([CH2:6][CH2:12][C:10](=[O:11])[CH:8]=[CH:9]2)[CH2:5][CH2:4][CH2:3]1

参加物

6

反応条件

温度
45 °C

実験手順

To a solution of cyclopentanecarbaldehyde (Aldrich) (0.82 g, 8.36 mmol) in dry toluene (10 mL), methyl vinyl ketone (Alfa Aesar) (0.684 mL, 8.36 mmol) was added followed by a catalytic amount of concentrated H2SO4 (0.045 mL, 0.836 mmol). The mixture was heated at 45° C. for 1.5 hours, then refluxed for 1 hour using a Dean-Stark trap. The reaction mixture was cooled to room temperature and further methyl vinyl ketone (Alfa Aesar) (0.684 mL, 8.36 mmol) was added. The reaction mixture was heated at reflux for 1 hour, allowed to cool to room temperature and treated with an aqueous 1M NaHCO3 (30 mL) solution. The aqueous was extracted with toluene and the combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude material was adsorbed onto silica and purification by chromatography eluting with 0-20% EtOAc in iso-hexane afforded the title compound;

後処理

  1. temperaturerefluxed for 1 hour
  2. temperatureThe reaction mixture was cooled to room temperature
  3. temperatureThe reaction mixture was heated
  4. temperatureat reflux for 1 hour
  5. temperatureto cool to room temperature
  6. extractionThe aqueous was extracted with toluene
  7. washthe combined organic extracts were washed with brine
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe crude material was adsorbed onto silica and purification by chromatography
  12. washeluting with 0-20% EtOAc in iso-hexane

出典と根拠

ORDレコード
ord-8920412465434c25af786424ec00ddb1
出典データセット
uspto-grants-2016_08
特許番号
US09403810B2

関連ノート

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