3-Allyl-4-methyl-4,5-epoxypentan-2-one → 2,4-Dimethyl-3-(prop-2-en-1-yl)furan
反応式
[CH2:1]([CH:4]([C:8]1([CH3:11])[O:10][CH2:9]1)[C:5](=O)[CH3:6])[CH:2]=[CH2:3]>C(=O)([O-])[O-].[Na+].[Na+]>[CH3:11][C:8]1[O:10][CH:9]=[C:5]([CH3:6])[C:4]=1[CH2:1][CH:2]=[CH2:3]参加物
3
実験手順
3-Allyl-4-methyl-4,5-epoxy-pentan-2-one (4.50 g) was added to a 1% aqueous sodium carbonate solution (150 ml), followed by stirring for 2 hours at a bath temperature of 60° to 65° C. The reaction solution was extracted three times with methylene chloride, and the methylene chloride layer was washed with an aqueous sodium chloride solution. After removing the solvent by evaporation, the residue was column chromatographed on silica gel (50 g) and developed with methylene chloride. From the first eluate (400 ml) was obtained 1.80 g of a pure objective 2,4-dimethyl-3-allylfuran.
後処理
- extractionThe reaction solution was extracted three times with methylene chloride
- washthe methylene chloride layer was washed with an aqueous sodium chloride solution
- customAfter removing the solvent
- customby evaporation
- customchromatographed on silica gel (50 g)
出典と根拠
- ORDレコード
- ord-6e38610a068c406181689ecfda0b98dd
- 出典データセット
- uspto-grants-1981_08
- 特許番号
- US04282372
反応ノート
読み込み中…