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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008658Generated: October 30, 2026

Iodine → 3-iodo-9H-carbazole

https://huagongshe.com/reaction/1008658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantCarbazoleHCID 6854—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product3-iodo-9H-carbazoleHCID 3678069140.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07972792B2
Source datasetuspto-grants-2011_07
ORD IDord-4017f5970f0b41a1af1bac5700e2c726
Source noteuspto-grants-2011_07