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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912249Generated: October 30, 2026

Chlorosuccinimide → 4-Chloro-2-methoxypyridine

https://huagongshe.com/reaction/1912249

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 numberUS08609150B2
Source datasetuspto-grants-2013_12
ORD IDord-6e510917648748f9943492a2b44072f9
Source noteuspto-grants-2013_12