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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Chloro-2-methoxy-4-methylpyridine | HCID 23133646 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-5-chloro-2-methoxy-4-methylpyridine | HCID 23133645 | 97.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653277B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-51eecb1ac836429fad7eb7296422825d |
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| Source note | uspto-grants-2014_02 |
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