Basic information Safety Supplier Related

4-Iododibenzo-[b,d]furan

Basic information Safety Supplier Related

4-Iododibenzo-[b,d]furan Basic information

Product Name:
4-Iododibenzo-[b,d]furan
Synonyms:
  • 4-Iododibenzo-[b,d]furan
  • 4-Iododibenzofuran
  • Dibenzofuran, 4-iodo-
  • iodo-Dibenzofuran
  • 4-iodobenzodifuran
CAS:
65344-26-5
MF:
C12H7IO
MW:
294.09
Mol File:
65344-26-5.mol
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4-Iododibenzo-[b,d]furan Chemical Properties

Melting point:
73°C(lit.)
Boiling point:
366.6±15.0 °C(Predicted)
Density 
1.809±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Light yellow
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Safety Information

HS Code 
2932.99.7000
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4-Iododibenzo-[b,d]furan Usage And Synthesis

Synthesis

132-64-9

65344-26-5

General procedure for the synthesis of 4-iododibenzofuran from dibenzofuran: 20 g (55 mmol) of dibenzofuran and 200 mL of tetrahydrofuran were added to a 500 mL three-necked flask, and a magnetic stirrer was turned on to mix the ingredients thoroughly. After the reaction system was cooled to -78 °C, 41 mL (66 mmol) of 1.6 M n-butyllithium hexane solution was slowly added dropwise, and the rate of dropwise acceleration was controlled to avoid violent exotherm. After the dropwise addition, the reaction mixture was gradually warmed up to room temperature with continuous stirring for 4 hours. The reaction system was again cooled to -78 °C and 16.7 g (66 mmol) of iodine monomer was added, followed by warming to room temperature and continued stirring for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of an appropriate amount of aqueous sodium thiosulfate and separated by extraction with ethyl acetate and deionized water. The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The crude product was purified by recrystallization to give 20.4 g of 4-iododibenzofuran in white crystalline form in 91% yield.

References

[1] Patent: KR2017/55704, 2017, A. Location in patent: Paragraph 0079-0085
[2] Synthesis (Germany), 2017, vol. 49, # 19, p. 4500 - 4516
[3] Patent: KR2015/124677, 2015, A. Location in patent: Paragraph 0321-0325
[4] Patent: EP2594573, 2013, A1. Location in patent: Paragraph 0105
[5] Patent: KR2015/114636, 2015, A. Location in patent: Paragraph 0393-0398

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