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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661571Generated: October 25, 2026

Sodium Iodide → 2-Iodoquinoline

https://huagongshe.com/reaction/661571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetyl chlorideHCID 6367—
Reactant2-ChloroquinolineHCID 11928—
SolventAcetonitrileHCID 6342—
Product2-IodoquinolineHCID 8104470%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Iodoquinoline was prepared according to the procedure of Kimber, et. al. (Tetrahedron 2000, 56, 3575). To a solution of 2-chloroquinoline (10.0 g, 61.5 mmol) in CH3CN (100 mL) was added sodium iodide (14 g, 92.3 mmol) and acetyl chloride (8.8 mL, 123 mmol). The reaction mixture was stirred at 100° C. for 5 hours, then cooled to room temperature and quenched with 10% aqueous K2CO3 (100 mL) and 5% aqueous NaHSO3 (50 mL). The aqueous layer was extracted twice with dichloromethane then the combined organic extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (0% to 20% EtOAc in hexanes) to provide 9.7 g (70%) of 2-iodoquinoline as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084623B2
Source datasetuspto-grants-2011_12
ORD IDord-0e2ad7a8c24944d5ba4f9e2f0eb10044
Source noteuspto-grants-2011_12