HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Ethyl 2-[2-cyano-5-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)benzimidazol-1-yl]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-bromopropionate | HCID 79040 | — |
| Reactant | HCID 19086710 | HCID 19086710 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 2-[2-cyano-5-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)benzimidazol-1-yl]propionate | HCID 19086745 | — |
| Product | HCID 19086747 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05306692 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-5ee0762d810748b885fd684198e0eb0a |
| Source note | uspto-grants-1994_04 |