1-(5-Allylbenzo[d][1,3]dioxol-2-yl)ethanone → 1-(5-(Prop-1-enyl)benzo[d][1,3]dioxol-2-yl)ethanone
反応式
[CH2:1]([C:4]1[CH:15]=[CH:14][C:7]2[O:8][CH:9]([C:11](=[O:13])[CH3:12])[O:10][C:6]=2[CH:5]=1)[CH:2]=[CH2:3]>CC1C=CC=CC=1C.C/C(/O)=C/C(C)=O.C/C(/O)=C/C(C)=O.C/C(/O)=C/C(C)=O.[Ru]>[CH:1]([C:4]1[CH:15]=[CH:14][C:7]2[O:8][CH:9]([C:11](=[O:13])[CH3:12])[O:10][C:6]=2[CH:5]=1)=[CH:2][CH3:3]参加物
4
実験手順
3.4 g of 1-(5-allylbenzo[d][1,3]dioxol-2-yl)ethanone and 68 mg (1 mol %) of ruthenium (III) acetylacetonate in 20 ml of o-xylene were stirred 2 days at 130° C., then cooled to room temperature. After concentration of the solvent in vacuum, the crude product was purified by flash chromatography on silica gel to give 1.3 g (38%) of a colorless oil.
後処理
- customAfter concentration of the solvent in vacuum, the crude product was purified by flash chromatography on silica gel
出典と根拠
- ORDレコード
- ord-e95b393b1c104ba3b527c7323cd1628a
- 出典データセット
- uspto-grants-2016_07
- 特許番号
- US09382500B2
反応ノート
読み込み中…