反応式
[Br:1]NC(=O)C.[CH:6]([Si:9]([CH:25]([CH3:27])[CH3:26])([CH:22]([CH3:24])[CH3:23])[O:10][CH:11]1[C:17]2=[N:18][CH:19]=[CH:20][CH:21]=[C:16]2[CH:15]=[CH:14][CH2:13][CH2:12]1)([CH3:8])[CH3:7].[C:28]([O-:31])(=[O:30])[CH3:29].[Li+]>CC(O)=O>[C:28]([O:31][CH:15]1[C:16]2[C:17](=[N:18][CH:19]=[CH:20][CH:21]=2)[CH:11]([O:10][Si:9]([CH:6]([CH3:8])[CH3:7])([CH:22]([CH3:24])[CH3:23])[CH:25]([CH3:27])[CH3:26])[CH2:12][CH2:13][CH:14]1[Br:1])(=[O:30])[CH3:29]参加物
5
実験手順
N-bromoacetamide (2.021 g, 14.65 mmol) was added to the AcOH (100 mL) suspension of (Z)-9-(triisopropylsilyloxy)-8,9-dihydro-7H-cyclohepta[b]pyridine (4.5597 g, 14.36 mmol) and LITHIUM ACETATE (3.79 g, 57.4 mmol) at rt under N2. The flask was wrapped with alumina foil and stirred at room temperature overnight. The reaction became a clear yellow solution. The solvent was evaporated via high vacuum. The crude was partitioned between water and ethyl acetate. Na2CO3 was added until no bubbling. The organic was separated and the aqueous was extract by ethyl acetate again. The combined organic layer was dried (Na2SO4), filtered and concentrated to give a tan oil (crude product: 6.37 g). The crude was used as it is. MS (ESI)[M+H+]=458.36.
後処理
- customThe solvent was evaporated via high vacuum
- customThe crude was partitioned between water and ethyl acetate
- additionNa2CO3 was added until no bubbling
- customThe organic was separated
- extractionthe aqueous was extract by ethyl acetate again
- dry with materialThe combined organic layer was dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customto give a tan oil (crude product: 6.37 g)
出典と根拠
- ORDレコード
- ord-28af8d81559a4920a5df1a907b25731b
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08143403B2
関連ノート
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