Methane → 4-benzyloxy-7-(2-ethoxy-1,2-dihydroxy-ethyl)-3H-benzoxazol-2-one
反応式
[C:1]([C:4]1[C:12]2[O:11][C:10](=[O:13])[NH:9][C:8]=2[C:7]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:6][CH:5]=1)(=[O:3])[CH3:2].[Se](=O)=O.[OH2:25].C.[O:27]1CCO[CH2:29][CH2:28]1>>[CH2:15]([O:14][C:7]1[C:8]2[NH:9][C:10](=[O:13])[O:11][C:12]=2[C:4]([CH:1]([OH:3])[CH:2]([O:27][CH2:28][CH3:29])[OH:25])=[CH:5][CH:6]=1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1参加物
6
実験手順
49.5 g (175 mmol) 7-acetyl-4-benzyloxy-3H-benzoxazol-2-one and 19.6 g (177 mmol) selenium dioxide are refluxed for 8 hours in 200 mL dioxane and 8 mL water in the presence of activated charcoal. The insoluble constituents are suction filtered, the solvent is distilled off and the residue is combined with 150 mL ethanol. The mixture is refluxed for 30 minutes and then filtered through activated charcoal. After the addition of a crystallisation aid the product is precipitated out of the cooled solution. It is suction filtered and washed with ethanol and diethyl ether.
後処理
- distillationthe solvent is distilled off
- temperatureThe mixture is refluxed for 30 minutes
- filtrationfiltered through activated charcoal
- additionAfter the addition of a crystallisation aid the product
- customis precipitated out of the cooled solution
- filtrationfiltered
- washwashed with ethanol and diethyl ether
出典と根拠
- ORDレコード
- ord-8ba1d6962c1e4e41bc73f1a36ab760df
- 出典データセット
- uspto-grants-2007_12
- 特許番号
- US07307076B2
反応ノート
読み込み中…