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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468093Generated: October 31, 2026

Sodium Carbonate → HCID 178506264, compound

https://huagongshe.com/reaction/1468093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5,6-Dichloro-2-trifluoromethylbenzimidazoleHCID 16859—
Reactant1,4-DioxaneHCID 31275—
Reactant3,4-Dichlorobenzeneboronic acidHCID 2734330—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 178506264HCID 178506264—

Reaction Conditions

Temperature100 °C

Reaction Steps

Compound number 258 (i.e., 6-chloro-5-(3,4-dichlorophenyl)-2-trifluoromethylbenzimidazole) was prepared as follows. A 100-mL round-bottom flask was purged and maintained with an inert atmosphere of nitrogen. 5,6-dichloro-2-(trifluoromethyl)-1H-1,3-benzodiazole (200 mg, 0.78 mmol, 1.00 equiv), 1,4-dioxane (30 mL), (3,4-dichlorophenyl)boronic acid (229 mg, 1.20 mmol, 2.00 equiv), sodium carbonate (191 mg), water (8 mL) and Pd(PPh3)4 (34.7 mg) was placed into the flask. The resulting solution was stirred overnight at 100° C. in an oil bath. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:4). This resulted in 82.4 mg (29%) of 6-chloro-5-(3,4-dichlorophenyl)-2-trifluoromethylbenzimidazole as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000187B2
Source datasetuspto-grants-2015_04
ORD IDord-4ca3a08d94e14008a2b8ff73e0d0c505
Source noteuspto-grants-2015_04