Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464582Generated: October 30, 2026

Potassium Carbonate → Ethyl 2-[2-cyano-5-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)benzimidazol-1-yl]propionate

https://huagongshe.com/reaction/1464582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-bromopropionateHCID 79040—
ReactantHCID 19086710HCID 19086710—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-[2-cyano-5-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)benzimidazol-1-yl]propionateHCID 19086745—
ProductHCID 19086747HCID 19086747—

Reaction Steps

2-Cyano-5-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)benzimidazole (0.325 g), ethyl 2-bromopropionate (0.13cm3) and anhydrous potassium carbonate (1 g) were heated under reflux in acetonitrile (30cm3) for 2 hours and left at room temperature overnight. The mixture was filtered and the solvent removed from the filtrate under vacuum. The residue was purified by preparative plate chromatography (SiO2 ; hexane:ether,1:1) to yield ethyl 2-[2-cyano-6-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)benzimidazol-1-yl]-propionate (0.14 g) as the faster component (compound 101) and ethyl 2-[2-cyano-5-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)benzimidazol-1-yl]propionate (0.15 g) as the slower component (compound 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05306692
Source datasetuspto-grants-1994_04
ORD IDord-5ee0762d810748b885fd684198e0eb0a
Source noteuspto-grants-1994_04