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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661809Generated: October 28, 2026

Sodium Iodide → 6-Iodoquinoline

https://huagongshe.com/reaction/1661809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant6-BromoquinolineHCID 79243—
Reactant1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product6-IodoquinolineHCID 20398553—

Reaction Conditions

Temperature110 °C

Reaction Steps

Sodium iodide (4.32 g, 28.8 mmol), Copper (I) iodide (137 mg, 0.72 mmol) and N,N′-Dimethyl-cyclohexane-1,2-diamine (0.227 mL, 1.44 mmol) and 6-Bromoquinoline (3 g, 14.4 mmol) in dioxane (15 mL) were charged in a 25 mL microwave tube. The tube was flushed with Nitrogen and sealed with a Teflon septum and Nitrogen was bubbled in the solution for 10 minutes, allowing the gas to escape through a needle. After the removal of the needle, the reaction mixture was stirred at 110° C. for 15 hours. Then, the green suspension was allowed to reach room temperature, poured into ice-water and extracted with dichloromethane. The organic layer was collected, dried (MgSO4), filtered and concentrated in vacuum. The crude mixture was chromatographied over silica gel with CH2Cl2 100% and CH2Cl2/MeOH:95/5 to yield 3.56 g (97%) of 6-Todoquinoline as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030305B2
Source datasetuspto-grants-2011_10
ORD IDord-a81b7a1e5c0649e7ad4cf6eac8edb27e
Source noteuspto-grants-2011_10