反応式
[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][C:2]1=[O:11].[I:12]I>C(O)C.S([O-])([O-])(=O)=O.[Ag+].[Ag+]>[I:12][C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[NH:1][C:2](=[O:11])[CH2:3][CH2:4]2参加物
5
実験手順
3,4-Dihydroquinolin-2(1H)-one (7.5 g; 51 mmol) and silver (I) sulfate (17.5 g; 56.1 mmol) were suspended in ethanol (250 mL). A solution of iodine in ethanol (250 mL) was added slowly to the reaction over 1 hour. After 6 hours, the reaction was filtered through CELITE diatomaceous earth and washed copiously with methanol. The volatiles were removed under vacuum and the crude residue was triturated with ether. The solids were collected on a fritted funnel and dried under vacuum. This provided the title compound.
後処理
- filtrationthe reaction was filtered through CELITE diatomaceous earth
- washwashed copiously with methanol
- customThe volatiles were removed under vacuum
- customthe crude residue was triturated with ether
- customThe solids were collected on a fritted funnel
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-d57d16896f9f4187ad5a58a2a543f654
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07084156B2
関連ノート
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