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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243771Generated: October 26, 2026

Sodium Thiosulfate → 3-Bromo-5-chloro-2-methoxy-4-methylpyridine

https://huagongshe.com/reaction/243771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Chloro-2-methoxy-4-methylpyridineHCID 23133646—
SolventDimethylformamideHCID 6228—
Product3-Bromo-5-chloro-2-methoxy-4-methylpyridineHCID 2313364597.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

20.2 g (114 mmol) of N-bromosuccinimide was charged to a N,N-dimethylformamide (DMF) 15 ml solution of 7.2 g (46 mmol) of 5-chloro-2-methoxy-4-methylpyridine, followed by stirring at 50° C. for 20 hours. A diluted sodium thiosulfate aqueous solution was added to the reaction solution, and the aqueous layer was extracted with diethyl ether. The organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate and subjected to filtration on the pad of a silica gel cake, and the solvent was distilled off under reduced pressure to obtain 10.6 g (yield: 97%) of 3-bromo-5-chloro-2-methoxy-4-methylpyridine (melting point: 44 to 45° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653277B2
Source datasetuspto-grants-2014_02
ORD IDord-51eecb1ac836429fad7eb7296422825d
Source noteuspto-grants-2014_02