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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352791Generated: October 27, 2026

Acetyl bromide → 4-Bromo-2,3-dimethylpyridine 1-oxide

https://huagongshe.com/reaction/352791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl bromideHCID 10482—
Reactant2,3-Dimethyl-4-nitropyridine-N-oxideHCID 148223—
ReactantAmmonium CarbonateHCID 517111—
Product4-Bromo-2,3-dimethylpyridine 1-oxideHCID 58997427—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 2,3-Dimethyl-4-nitropyridine N-oxide (3.00 g) which had been cooled to 0° C., added was acetyl bromide (18.0 ml), followed by stirring at 50° C. for 20 minutes and then at 75° C. for 15 minutes. The reaction mixture was charged in ice water and neutralized with an aqueous solution of ammonium carbonate. The neutralized solution was separated using methylene chloride. The organic layer was dried over anhydrous sodium sulfate and the filtrate was concentrated, whereby a crudely purified product of 4-bromo-2,3-dimethylpyridine N-oxide was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-8c6fda6a51f14930bce16d968b15977c
Source noteuspto-grants-2004_06