反応式
C[Si]([C:5]#[C:6][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[CH:13]=[C:12]([OH:17])[CH:11]=[CH:10]2)(C)C.C([O-])([O-])=O.[K+].[K+]>CO.C1COCC1.C(OCC)(=O)C>[C:6]([C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][CH:16]=1)[CH:13]=[C:12]([OH:17])[CH:11]=[CH:10]2)#[CH:5]参加物
6
実験手順
Compound 110A (770 mg, 3.20 mmol) in MeOH (5 ml) and THF (10 ml) was treated with K2CO3 (885 mg, 6.41 mmol) at room temperature for 3 h. The reaction was diluted with ethyl acetate and washed with water. The organic layer was concentrated and the residue was purified by flash chromatography, eluted with DCM to provide the compound 110B.
後処理
- washwashed with water
- concentrationThe organic layer was concentrated
- customthe residue was purified by flash chromatography
- washeluted with DCM
出典と根拠
- ORDレコード
- ord-b26daf207e0a4777895a4cc24c021b56
- 出典データセット
- uspto-grants-2012_07
- 特許番号
- US08232273B2
関連ノート
読み込み中…