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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120103Generated: November 1, 2026

Water → 2-Acetamido-5-bromopyridine

https://huagongshe.com/reaction/2120103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetyl chlorideHCID 6367—
Reactant2-Amino-5-bromopyridineHCID 70622—
SolventPyridineHCID 1049—
Product2-Acetamido-5-bromopyridineHCID 29309785%

Reaction Steps

In 29 ml of pyridine was dissolved 1 g of 2-amino-5-bromopyridine which was then acetylated through reaction with 0.61 ml of acetyl chloride at room temperature for 15 hours with stirring. Following the addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer thus obtained was washed with brine. Dehydration, filtration and concentration under vacuum of the organic layer provided a solid which was then recrystallized in ethanol and hexane to obtain the title compound. 1.06 g. Yield 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689779B2
Source datasetuspto-grants-2004_02
ORD IDord-24d236d01ae64950970b90f4d845cb0f
Source noteuspto-grants-2004_02