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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189899Generated: October 26, 2026

Iodine → 2,6-Dichloro-5-fluoro-4-iodonicotinonitrile

https://huagongshe.com/reaction/2189899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDiisopropylamineHCID 7912—
ReactantSodium ThiosulfateHCID 24477—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2,6-Dichloro-5-fluoro-3-pyridinecarbonitrileHCID 2733849—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2,6-Dichloro-5-fluoro-4-iodonicotinonitrileHCID 8662062387.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of diisopropylamine (15.9 g, 157 mmol) in THF (400 ml) at −78° C. was added n-butyllithium (2.5 M hexanes, 154 mmol), and the solution was stirred at −78° C. for 30 minutes. The lithium diisopropylamide solution was then added slowly dropwise to a −78° C. solution of 2,6-dichloro-5-fluoronicotinonitrile (10.0 g, 52.3 mmol) and iodine (26.5 g, 104 mmol) in THF (175 ml). Upon completion of the addition, the reaction was allowed to warm slowly to room temperature, and stirred at room temperature for 12 hours. An aqueous 10% Na2S2O3 solution (500 ml) was added and the reaction was extracted with EtOAc (3×300 ml). The combined organic fractions were dried over Na2SO4, filtered, and then concentrated to give the title compound (14.5 g, 87%) as a brown solid that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324252B2
Source datasetuspto-grants-2012_12
ORD IDord-49c314c1e7fe4cf8a22b7b76078aeca1
Source noteuspto-grants-2012_12