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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820934Generated: October 25, 2026

Sodium Acetate → N-(5-chloropyridin-2-yl)-2-acetoxyacetamide

https://huagongshe.com/reaction/1820934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant2-chloro-N-(5-chloropyridin-2-yl)acetamideHCID 5151148—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(5-chloropyridin-2-yl)-2-acetoxyacetamideHCID 2306265289.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Chloro-N-(5-chloropyridin-2-yl)acetamide (30.68 g) obtained in Reference Example 26(1) is dissolved in N,N-dimethylformamide (500 ml), thereto is added sodium acetate (24.55 g), and the mixture is stirred at 60° C. for 5 hours. The reaction solution is diluted with ethyl acetate, washed successively with water and saturated brine. The solution is dried over magnesium sulfate, treated with activated charcoal, and the filtrate is concentrated under reduced pressure. The resulting residue is suspended in n-hexane and crystals are collected by filtration, washed with n-hexane, and dried to give N-(5-chloropyridin-2-yl)-2-acetoxyacetamide (30.58 g). APCI-MS M/Z:229/231[M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605158B2
Source datasetuspto-grants-2009_10
ORD IDord-69929170c9814fa581953b4d1a5fee46
Source noteuspto-grants-2009_10