Reacción #1095840

ord-4017f5970f0b41a1af1bac5700e2c726

Ecuación de reacción

c1ccc2c(c1)[nH]c1ccccc12
carbazole
II
I2
[Na+].[OH-]
NaOH
O=S(=O)(O)O
H2SO4
Ic1ccc2[nH]c3ccccc3c2c1
compound 1
Rendimiento 140.1%
Ic1ccc2[nH]c3ccccc3c2c1
3-Iodocarbazole
Rendimiento 140.1%

Reactivos

Ninguno

Condiciones de reacción

Temperatura
65°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroEthanol was removed
  2. 2
    Extracciónthe reaction solution was extracted two times with chloroform
  3. 3
    LavadoThe extract was washed two times with water
  4. 4
    SecadoThe organic phase was dried over Na2SO4
  5. 5
    Otrothe solvent was removed
  6. 6
    OtroThe residue was purified by column chromatography (HexH:AcOEt=4:1)

Procedimiento

To an ethanol solution (500 mL) of carbazole (2.50 g, 15.0 mmol), NaIO4 (0.80 g, 3.75 mmol) and I2 (1.89 g, 7.45 mmol) were sequentially added, and then an ethanol solution (100 mL) of H2SO4 (1.60 mL, 30.0 mmol) was added. The reaction solution was refluxed for one hour at 65° C. The loss of raw materials was confirmed by TLC (HexH:AcOEt=4:1), and an ethanol solution (100 mL) of NaOH (1.4 g) was added thereto to neutralize the system. Ethanol was removed, and then the reaction solution was extracted two times with chloroform. The extract was washed two times with water. The organic phase was dried over Na2SO4, and the solvent was removed. The residue was purified by column chromatography (HexH:AcOEt=4:1), and thus compound 1 (3.06 g, 70%) was obtained as a white powder. Thus, 3,6-diiodocarbazole (0.47 g, 7.5%) was obtained as a white powder.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07972792B2uspto-grants-2011_07