反応式
[C:1]1([C:7]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)([CH2:12][CH2:13][CH2:14][CH:15]=[CH2:16])[CH:8]([OH:11])[CH2:9][CH3:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cr](O)(O)(=O)=O>CC(C)=O>[C:17]1([C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)([CH2:12][CH2:13][CH2:14][CH:15]=[CH2:16])[C:8](=[O:11])[CH2:9][CH3:10])[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1参加物
4
実験手順
One hundred seventy milligrams of 4,4-diphenylnon-8-en-3-ol was dissolved in acetone (10 ml), and then treated with 2.7M chromic acid solution (0.04 ml). After 10 min, the excess oxidant was destroyed with isopropanol, and the mixture was diluted with ether (20 ml). Filtration through a pad of celite and concentration yielded 133 mg of 4,4-diphenylnon-8-en-3-one, as an amorphous white solid.
後処理
- customthe excess oxidant was destroyed with isopropanol
- additionthe mixture was diluted with ether (20 ml)
- filtrationFiltration
- concentrationthrough a pad of celite and concentration
出典と根拠
- ORDレコード
- ord-ed73cb74f4f64592b7d42a4b31c17767
- 出典データセット
- uspto-grants-1991_12
- 特許番号
- US05073629
関連ノート
読み込み中…