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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425266Generated: November 3, 2026

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

https://huagongshe.com/reaction/1425266

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 numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-f449ebb9566c4b889df152e08339299c
Source noteuspto-grants-2015_01