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

HRID 1432037
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HRID 1432037 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

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.

후처리

  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.

출처 및 근거

ORD 기록
ord-86dd5d4d1e75444d9e018dbf24cbbe0c
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07612068B2

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