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Iodine → 4-Bromo-2-iodo-1-methoxybenzene

HRID 1432037
ノート
印刷プレビュー

反応式

HRID 1432037 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=1.C(O)(=O)C.C(O)(=O)C.[I:18]C1C=CC=CC=1.II.[O-]S([O-])(=S)=O.[Na+].[Na+]>C(#N)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[C:4]([I:18])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 807IodineHCID 77304-BromoanisoleHCID 24477Sodium ThiosulfateHCID 12217721Iodo benzene diacetate

生成物 1

HCID 109799044-Bromo-2-iodo-1-methoxybenzene

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

4-Bromo-anisole (4.417 g, 23.6 mmol) was dissolved in acetonitrile (200 mL) and placed under an argon atmosphere in the absence of light. Iodobenzene diacetate (9.18 g, 28.5 mmol) was added followed by iodine (3.6 g, 14.2 mmol). The mixture was stirred for 16 hours at ambient temperature. The mixture was then poured into 1M Na2S2O3 (200 mL) and stirred until the solution was colourless. The solution was then extracted with diethyl ether (3×100 mL). The combined organic extracts were then washed with brine, dried with Na2SO4, filtered and evaporated to dryness. The crude product was filtered through a silica gel plug eluting with heptane/ethyl acetate (3:1) (200 mL). The filtrate was concentrated and the residue was distilled using a Kugelrohr apparatus collecting the compound at 75° C., 0.01 mbar.

後処理

  1. stirringstirred until the solution
  2. extractionThe solution was then extracted with diethyl ether (3×100 mL)
  3. washThe combined organic extracts were then washed with brine
  4. dry with materialdried with Na2SO4
  5. filtrationfiltered
  6. customevaporated to dryness
  7. filtrationThe crude product was filtered through a silica gel plug
  8. washeluting with heptane/ethyl acetate (3:1) (200 mL)
  9. concentrationThe filtrate was concentrated
  10. distillationthe residue was distilled
  11. customcollecting the compound at 75° C.

出典と根拠

ORDレコード
ord-86dd5d4d1e75444d9e018dbf24cbbe0c
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07612068B2

反応ノート

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