反応式
FC(F)(F)[C:3]([OH:5])=[O:4].C(C1C=CC(N[CH:18]([C:34]2[CH:39]=[C:38]([O:40][CH3:41])[C:37](OC)=C[C:35]=2F)C2NC(=O)N(C3C=CC=CC=3C(O)=O)N=2)=CC=1)(=N)N.[H-].[Na+].[Br:47][CH2:48]Cl.[I-].[Na+].[Cl-].[NH4+].[CH3:54]N(C=O)C>C(OCC)(=O)C>[Br:47][C:48]1[CH:37]=[C:38]([O:40][CH2:41][CH3:54])[C:39]2[O:5][CH2:3][O:4][CH2:18][C:34]=2[CH:35]=1参加物
反応物 6
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of this compound in 40 ml of DMF there was added 1g of sodium hydride (60% oily suspension) while cooling on ice, and the mixture was stirred at room temperature for 30 minutes. After then adding 1 ml of bromochloromethane and 0.25 g of sodium iodide to the reaction mixture, it was stirred at 80° C. for 6 hours under a hydrogen atmosphere. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give 6-bromo-8-ethoxy-4H-benzo[1,3]dioxine (1.62 g).
後処理
- temperaturewhile cooling on ice
- stirringwas stirred at 80° C. for 6 hours under a hydrogen atmosphere
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- filtrationThe desiccating agent was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- customThe residue was purified by silica gel column chromatography (ethyl acetate-heptane)
出典と根拠
- ORDレコード
- ord-035d2348da454e09b4cd0f7fbaefe427
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07928228B2
関連ノート
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