Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549211Generated: October 29, 2026

Iodine → 3-Fluoro-4-iodoquinoline

https://huagongshe.com/reaction/549211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDiisopropylamineHCID 7912—
Reactant3-FluoroquinolineHCID 96405—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Fluoro-4-iodoquinolineHCID 1110849641.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a 0° C. solution of diisopropyl amine (2.8 mL, 27 mmol) in tetrahydrofuran (80 mL) was added dropwise butyl lithium (8.1 mL, 2.5 M solution in hexane, 27 mmol). After 10 min., the flask was cooled to −78° C. and 3-fluoro quinoline from Step B (3 g, 20 mmol) in 20 mL of tetrahydrofuran was added over 15 min. period. The stirring was continued for an additional 4 h., after which iodine (5.4 g, 21 mmol) in 10 mL of THF (tetrahydrofuran) was added and the reaction temperature was maintained at −78° C. for additional 2 h. The reaction was quenched by adding a mixture of water and tetrahydrofuran (25 mL, 1:9), and the resulting solution was extracted with ethyl acetate. The organic layers were combined, washed with water and brine. Purification by silica gel column gave the title compound (2.26 g, 40%). MS (ES) 148.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943640B2
Source datasetuspto-grants-2011_05
ORD IDord-892ab906687644b099561ef291dc8527
Source noteuspto-grants-2011_05