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Dibenzofuran → 2-Iododibenzofuran

HRID 1747203
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인쇄 미리보기

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HRID 1747203 반응식
[CH:1]1[C:9]2[C:8]3[CH:10]=[CH:11][CH:12]=[CH:13][C:7]=3[O:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.II.[I:16](O)(O)(O)(O)(O)=O.S(=O)(=O)(O)O>O.C(O)(=O)C>[I:16][C:2]1[CH:3]=[CH:4][C:5]2[O:6][C:7]3[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=3[C:9]=2[CH:1]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 568DibenzofuranHCID 807IodineHCID 1118Sulfuric AcidHCID 25289Orthoperiodic acid

생성물 1

HCID 2233272-Iododibenzofuran수율 77%

시약·촉매·용매 2

HCID 176Acetic Acid용매
HCID 962
Water
용매

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온도
60 °C

실험 절차

In a 500-mL three-neck flask, a suspension of 8.4 g (50 mmol) of dibenzofuran, 6.2 g (25 mmol) of iodine, 5.7 g (25 mmol) of orthoperiodic acid, 150 mL of glacial acetic acid, 30 mL of water, and 500 μL of sulfuric acid was heated and stirred at 60° C. for 4.5 hours. After that, the mixture was stirred at room temperature for 16 hours. The generated precipitate was collected by filtration, and the resulting matter was dissolved in 150 mL of toluene and a toluene solution was made. This toluene solution was washed with water three times. After the washing, magnesium sulfate was added to the toluene solution to adsorb moisture. This mixture was filtered and the given filtrate was concentrated. After that, hexane was added, and the mixture was irradiated with ultrasonic waves to perform recrystallization, so that 11.3 g of white powder, which was the objective substance, was obtained in 77% yield. A synthetic scheme of Step 1 is shown in (a-1) below.

후처리

  1. temperaturewas heated
  2. stirringAfter that, the mixture was stirred at room temperature for 16 hours
  3. filtrationThe generated precipitate was collected by filtration
  4. dissolutionthe resulting matter was dissolved in 150 mL of toluene
  5. washThis toluene solution was washed with water three times
  6. additionAfter the washing, magnesium sulfate was added to the toluene solution
  7. filtrationThis mixture was filtered
  8. concentrationthe given filtrate was concentrated
  9. additionAfter that, hexane was added
  10. customthe mixture was irradiated with ultrasonic waves
  11. customrecrystallization
  12. customwas obtained in 77% yield

출처 및 근거

ORD 기록
ord-9963a8848be34ca0914785d1ab729213
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150551B2

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