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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284728Generated: October 31, 2026

Ethyl Acetate → HCID 90052275, compound

https://huagongshe.com/reaction/2284728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 90052266HCID 90052266—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 90052275HCID 90052275—

Reaction Steps

To a suspension of tert-butyl ((6-iodo-1H-benzo[d]imidazol-2-yl)methyl)carbamate (G4, 216 mg), bis(triphenylphosphine)palladium(II) dichloride (40 mg) and copper(I) iodide (22 mg) in tetrahydrofuran (2 mL), triethylamine (243 μL) and trimethylsilylacetylene (96 μL) were added at room temperature, and the mixture was stirred at the same temperature for 3 hours. To the reaction mixture, ethyl acetate and saturated aqueous sodium hydrogencarbonate were added. The organic layer was separated, washed with saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 70 to 0% hexane in ethyl acetate) to obtain tert-butyl ((6-((trimethylsilyl)ethynyl)-1H-benzo[d]imidazol-2-yl)methyl)carbamate (G5, 82 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-9d7be923c7bd47a0a83828eb95a50b61
Source noteuspto-grants-2015_09