Sodium Iodide → 1,4-Benzodioxin

HRID 1270424노트

반응식

HRID 1270424 반응식
Br[CH:2]1[O:7][C:6]2[CH:8]=[CH:9][CH:10]=[CH:11][C:5]=2[O:4][CH:3]1Br.[I-].[Na+]>CC(C)=O>[O:4]1[C:5]2[CH:11]=[CH:10][CH:9]=[CH:8][C:6]=2[O:7][CH:2]=[CH:3]1

참가 물질

4

반응물 2

HCID 5238Sodium IodideHCID 123986892,3-Dibromo-2,3-dihydro-1,4-benzodioxine

생성물 1

HCID 1360711,4-Benzodioxin

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

73.45 mmol of the compound obtained in Step A above are dissolved in 125 ml of acetone; the solution is then stirred for 2 hours under reflux, in the presence of sodium iodide (359.9 mmol). After evaporating off the solvent, the residue is dissolved in a mixture of water/ethyl acetate (100 ml/200 ml). The organic phase is then washed with 20% aqueous sodium thiosulphate solution and then the aqueous phase is extracted twice with ethyl acetate. The organic phases are combined, dried over magnesium sulphate and then concentrated to dryness. Purification by chromatography over silica gel (petroleum ether/ethyl acetate: 95/5) allows the expected product to be obtained.

후처리

  1. customAfter evaporating off the solvent
  2. dissolutionthe residue is dissolved in a mixture of water/ethyl acetate (100 ml/200 ml)
  3. washThe organic phase is then washed with 20% aqueous sodium thiosulphate solution
  4. extractionthe aqueous phase is extracted twice with ethyl acetate
  5. dry with materialdried over magnesium sulphate
  6. concentrationconcentrated to dryness
  7. customPurification by chromatography over silica gel (petroleum ether/ethyl acetate: 95/5)
  8. customto be obtained

출처 및 근거

ORD 기록
ord-24817b0c12f94929b546dbb40aa7b874
출처 데이터셋
uspto-grants-2007_04
특허 번호
US07202255B2

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