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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258340Generated: October 31, 2026

Acetyl bromide → 4-Bromo-2,5-dimethylpyridine 1-oxide

https://huagongshe.com/reaction/2258340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl bromideHCID 10482—
ReactantPyridine N-OxideHCID 12753—
ReactantSodium HydroxideHCID 14798—
Product4-Bromo-2,5-dimethylpyridine 1-oxideHCID 5444385993.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

A portion of the pyridine-N-oxide (106.4 g, 0.633 mol) was added slowly to 300 g of acetyl bromide at a rate that maintained the reaction temperature at 20°-30° C. (modification of procedure described in Ochiai, J. Org. Chem, 18, 549(1953)). After the addition was complete, the reaction was heated to 55° C. and left to stir overnight. The reaction mixture was cooled to room temperature and then slowly poured over ice. The mixture was slowly basified with 10M sodium hydroxide and extracted with chloroform. The chloroform extract was dried over sodium sulfate and then concentrated to dryness to give 119.2 g (93%) of 4-bromo-2,5-dimethylpyridine-N-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658908
Source datasetuspto-grants-1997_08
ORD IDord-1b5ac2fcec414084a4762999c9568b8b
Source noteuspto-grants-1997_08