Sodium Iodide → 6-bromo-8-ethoxy-4H-benzo[1,3]dioxine

HRID 2079153

反応式

HRID 2079153 の反応式
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

8

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

  1. temperaturewhile cooling on ice
  2. stirringwas stirred at 80° C. for 6 hours under a hydrogen atmosphere
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. filtrationThe desiccating agent was filtered off
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. 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

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