Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043927Generated: November 2, 2026

Isopropanol → 4-Iodo-2-isopropyloxy-3,5-dimethylpyridine

https://huagongshe.com/reaction/1043927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantSodium hydrideHCID 24758—
Reactant2-Fluoro-4-iodo-3,5-dimethylpyridineHCID 73554898—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Iodo-2-isopropyloxy-3,5-dimethylpyridineHCID 86686351—

Reaction Steps

Sodium hydride (60% oil dispersion, 191 mg) was added to a solution of IPA (0.77 mL) in THF (5 mL). After foaming was stopped, a solution of 2-fluoro-4-iodo-3,5-dimethylpyridine obtained in Preparation Example 29 (500 mg) in THF (5 mL) was added to the solution, and the mixture was stirred at mom temperature for two hours. The mixture was stirred at 50° C. for two hours, and the reaction mixture was then cooled to room temperature. The reaction mixture was cooled at 0° C., and MTBE (20 mL) and water (20 mL) were then added. The organic layer was separated. The organic layer was washed with brine. The combined aqueous layers were extracted with MTBE. The combined organic layers were dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to give the title compound (490 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563565B2
Source datasetuspto-grants-2013_10
ORD IDord-67ac975e7ff948c68a5c94a2516fef3c
Source noteuspto-grants-2013_10