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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824922Generated: October 30, 2026

Potassium Carbonate → HCID 22144870, compound

https://huagongshe.com/reaction/1824922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiethyl bromomalonateHCID 69637—
Reactant3-Bromo-2-hydroxy-5-nitrobenzaldehydeHCID 519307—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 22144870HCID 22144870108.1%

Reaction Steps

A mixture of 11.0 gm (44.7 mMol) 2-hydroxy-3-bromo-5-nitrobenzaldehyde, 5.56 gm (40.24 mMol) potassium carbonate, and 8.0 mL (46.95 mMol) diethyl bromomalonate in 55 mL 2-butanone was heated at reflux for 5 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was partitioned between 450 mL diethyl ether and 250 mL water and the aqueous phase was adjusted to pH of about 1 by the addition of dilute sulfuric acid. The phases were separated and the aqueous phase was extracted with two 150 mL portions of diethyl ether. The organic phases were combined, washed with 50 mL saturated aqueous sodium chloride, dried over magnesium sulfate and concentrated under reduced pressure. The residual solid was dissolved in 200 mL ethanol to which were added 4.8 gm (85.5 mMoL) potassium hydroxide. The resulting suspension was warmed on a steam bath for 1 hour. The suspension was then cooled to room temperature. After about 18 hours the mixture was filtered and dried under reduced pressure to provide 14.1 gm (98%) of the desired compound as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045545B1
Source datasetuspto-grants-2006_05
ORD IDord-f0d42ad8ab324eaaad2d53c5de86ea44
Source noteuspto-grants-2006_05