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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767415Generated: October 30, 2026

Ethyl bromoacetate → HCID 18317825, compound

https://huagongshe.com/reaction/1767415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Iodo-6-methylpyridin-3-olHCID 89957—
SolventAcetoneHCID 180—
ProductHCID 18317825HCID 1831782556.3%

Reaction Steps

The mixture of 6-iodo-2-picolin-5-ol (235 mg, 1.0 mmol), potassium carbonate (455 mg, 3.3 mmol), ethyl bromoacetate (250 mg, 1.49 mmol) and acetone (15 ml) was refluxed for 15 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 10 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the mixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 3, and then extracted three times with ethyl acetate (20 ml each). Organic phases were combined, washed with water and brine, dried over magnesium sulfate, filtered, and then evaporated in vacuo. The residue was recrystallized from ethanol and petroleum ether to give 165 mg 6-iodo-2-methylpyridine-5-oxyacetic acid as white crystals, mp 170-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039707E1
Source datasetuspto-grants-2007_06
ORD IDord-73ef7ffe7fa4445888dcaced88d53c24
Source noteuspto-grants-2007_06