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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243758Generated: October 25, 2026

Chlorosuccinimide → 4-Chloro-2-methoxypyridine

https://huagongshe.com/reaction/243758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant4-Iodo-2-methoxypyridineHCID 15019795—
ReactantHCID 178418918HCID 178418918—
ReactantHCID 178492981HCID 178492981—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-2-methoxypyridineHCID 22638510—

Reaction Conditions

Temperature0 °C

Reaction Steps

50.6 ml (2 mol/l tetrahydrofuran solution) of isopropylmagnesium chloride was cooled with ice, and a solution having 19.8 g (84.3 mmol) of crude 4-iodo-2-methoxypyridine obtained in Step (c) dissolved in 80 ml of tetrahydrofuran was added, followed by stirring at 0° C. for 1 hour and then at room temperature for 1 hour to prepare 2-methoxy-4-pyridylmagnesium chloride. Then, 16.9 g (127 mmol) of N-chlorosuccinimide was gradually added, followed by stirring at room temperature for 1 hour. 100 ml of water was added to terminate the reaction, and tetrahydrofuran was distilled off under reduced pressure. After extraction with ethyl ether, the organic layer was dried over sodium sulfate and subjected to filtration, and the solvent was distilled off under reduced pressure to obtain 11.0 g (crude yield: 91%) of crude 4-chloro-2-methoxypyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653277B2
Source datasetuspto-grants-2014_02
ORD IDord-175a2d8d66284e0ea4d7d35f60774473
Source noteuspto-grants-2014_02