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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448513Generated: October 29, 2026

Iodine → 3-iodo-9H-carbazole

https://huagongshe.com/reaction/448513

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 added in this order, and then an ethanol solution (100 mL) of H2SO4 (1.60 mL, 30.0 mmol) was added thereto. The reaction solution was heated to reflux for one hour at 65° C. Disappearance of the 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 reaction solution. Ethanol was removed, and then the reaction solution was extracted two times with chloroform and 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 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 numberUS08481714B2
Source datasetuspto-grants-2013_07
ORD IDord-a58ff5c1996b4579a6a102dcd94ce17c
Source noteuspto-grants-2013_07