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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640900Generated: October 27, 2026

Iodine → 2-Chloro-4-iodo-5-(methoxymethoxy)pyridine

https://huagongshe.com/reaction/1640900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-chloro-5-(MethoxyMethoxy)pyridineHCID 58764193—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-4-iodo-5-(methoxymethoxy)pyridineHCID 5876411558.2%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Add tert-buty lithium (1.7 M in pentane, 72 mL, 123 mmol) to a solution of 2-chloro-5-methoxymethoxy-pyridine (10.8 g, 62 mmol) in THF (300 mL) at −70° C. dropwise over 10 min. Stir the resulting solution at −70° C. for 30 min. Add a solution of iodine (23 g, 92 mmol) in THF (150 mL) dropwise over 30 min. Stir the resulting solution at −70° C. for 1 h. Remove the ice bath and allow the reaction to warm to RT. Dilute the mixture with ethyl acetate and water and isolate the phases. Extract the aqueous phase with two portions of ethyl acetate. Combine the organic extracts and wash with two portions of aqueous sodium thiosulfate, one portion of water, and one portion of saturated aqueous sodium chloride. Dry over sodium sulfate, filter, and evaporate. Triturate the resulting solid with hexane. Collect the solid by vacuum filtration and wash the solid with hexane. Dry the solid under vacuum to give the title compound 10.8 g (58%) as a brown solid. 1H NMR (400 MHz, DMSO-d6) δ 8.08 (s, 1H), 7.98 (s, 1H), 5.43 (s, 2H), 3.40 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114872B2
Source datasetuspto-grants-2012_02
ORD IDord-4e2d91f09e5346edb8742043b66a2ae9
Source noteuspto-grants-2012_02