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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43798Generated: October 29, 2026

Dimethylformamide → Ethyl 6-nitro-3-[(trimethylsilyl)ethynyl]-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/43798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantEthyl 3-bromo-6-nitro-1-benzothiophene-2-carboxylateHCID 67549192—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178419050HCID 178419050—
SolventTriethylamineHCID 8471—
ProductEthyl 6-nitro-3-[(trimethylsilyl)ethynyl]-1-benzothiophene-2-carboxylateHCID 67549085—

Reaction Conditions

Temperature80 °C

Reaction Steps

DMF (20 ml), (trimethylsilyl)acetylene (5 ml), triethylamine (10 ml) and bis(triphenylphosphine)palladium (II) dichloride (420 mg, 0.6 mmol) were added to ethyl 3-bromo-6-nitro-1-benzothiophene-2-carboxylate obtained in Example (183b) (794 mg, 2.41 mmol) and copper (I) iodide (12 mg, 0.63 mmol), and the mixture was stirred at 80° C. for one hour. The reaction solution was concentrated under reduced pressure, diluted with ethyl acetate, washed with dilute hydrochloric acid and brine, and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=1/10) and recrystallized from an ethyl acetate/hexane solvent, to obtain 110 mg of the title compound as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-47affd0451bc46d788ac3a5a5698813f
Source noteuspto-grants-2013_09