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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791867Generated: November 3, 2026

Ethyl bromoacetate → HCID 86584802, compound

https://huagongshe.com/reaction/1791867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22033496HCID 22033496—
SolventDimethylformamideHCID 6228—
ProductHCID 86584802HCID 86584802—

Reaction Steps

N-{3-[2-(4-Cyanophenyl)ethoxy]phenyl}benzenesulfonamide (0.179 g; 0.47 mmol; from Example 1(iv) above), K2CO3 (0.082 g; 0.59 mmol) and ethyl bromoacetate (63 μL; 0.57 mmol) were stirred in DMF (10 mL) for 1 hour at room temperature, then 1 hour at 60° C. The mixture was filtered and the solvent removed in vacuo. The residue was dissolved in EtOAc and washed with water. The aqueous phase was extracted with EtOAc. The combined organic portions were dried (Na2SO4) and the solvent evaporated to afford the sub-title compound in a quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074820B2
Source datasetuspto-grants-2006_07
ORD IDord-8b5caf0ce965422b920c209aacc255dd
Source noteuspto-grants-2006_07