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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393884Generated: October 31, 2026

Potassium Iodide → 3,6-Diiodo-9-(4-methoxyphenyl)carbazole

https://huagongshe.com/reaction/1393884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant9-(4-Methoxyphenyl)carbazoleHCID 3110802—
ReactantPotassium IodateHCID 23665710—
SolventAcetic AcidHCID 176—
Product3,6-Diiodo-9-(4-methoxyphenyl)carbazoleHCID 58389855—

Reaction Steps

Potassium iodate (16.05 g, 75 mmol, obtained from Aldrich) was added in one portion to a stirred mixture of 9-(4-methoxyphenyl)carbazole (9.54 g, 34 mmol), potassium iodide (10.96 g, 66 mmol), and acetic acid (100 ml) at 80° C. The reaction mixture was stirred and heated for 1 hour. After the reaction was completed, the acetic acid was removed by distillation. The residue was dissolved in ethyl acetate and washed several times with an aqueous solution of sodium bicarbonate. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated, and dried. The yield of 3,6-diiodo-9-(4-methoxyphenyl)carbazole was 16.07 g (87.6%). The 1H-NMR spectrum (100 MHz) of the product in CDCl3 was characterized by the following chemical shifts (δ, ppm): 4.04 (s, 3H, OCH3), 7.24-7.63 (m, 6H, Ar), 8.35-8.40 (m, 4H, Ar). The mass spectrum of the product was characterized by the following ions (in m/z): 525 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348116B2
Source datasetuspto-grants-2008_03
ORD IDord-f635a731d740426cb6991944a2639e0c
Source noteuspto-grants-2008_03