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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818898Generated: October 26, 2026

Trifluoroacetic acid → 5-Iodo-2-methoxy-4,6-dimethylpyridine-3-carbonitrile

https://huagongshe.com/reaction/1818898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
ReactantSodium ThiosulfateHCID 24477—
ReactantN-IodosuccinimideHCID 120273—
Reactant2-Methoxy-4,6-dimethylnicotinonitrileHCID 595276—
SolventDichloromethaneHCID 6344—
Product5-Iodo-2-methoxy-4,6-dimethylpyridine-3-carbonitrileHCID 5677751194%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-methoxy-4,6-dimethyl-nicotinonitrile (1.0 g, 6.166 mmol) was disolved in 30 mL of anhydrous methylene chloride and then added with 6 mL of trifluoro acetic acid and N-iodosuccinimide (2.2 g, 9.248 mmol) in this order while stirring at 0° C. under the nitrogen atmosphere and then stirred again at room temperature for about 4 hours. The mixture was added with 60 mL of a saturated solution of sodium carbonate and 60 mL of a saturated solution of Na2S2O3 and then extracted twice with 80 mL of methylene chloride. The resulting organic layer was dried with anhydrous sodium sulfate, and filtered. A silica gel column chromatography (5% EtOAc/Hexanes) was performed on the resulting residue and 1.67 g (94%) of 5-iodo-2-methoxy-4,6-dimethyl-nicotinonitrile was obtained in white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601736B2
Source datasetuspto-grants-2009_10
ORD IDord-56a9e0467fdb4389a6edcbf97db599b3
Source noteuspto-grants-2009_10