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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400274Generated: November 1, 2026

Triethylamine → HCID 69096929, compound

https://huagongshe.com/reaction/2400274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylacetyleneHCID 10821—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86665746HCID 86665746—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventAcetonitrileHCID 6342—
ProductHCID 69096929HCID 69096929—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of N-(2-bromo-5-chloro-4-methoxyphenyl)-2,2,2-trifluoroacetamide (512 mg), phenylacetylene (0.254 mL), copper(I) iodide (17.5 mg), triethylamine (0.549 mL), and acetonitrile (12.3 mL) was added bis(triphenylphosphine) palladium(II) dichloride (32.5 mg). The mixture was stirred at 120° C. for 2 hours under microwave irradiation. The reaction mixture was left to cool. To the reaction mixture was added potassium carbonate (532 mg). The mixture was stirred at 120° C. for 2 more hours under microwave irradiation. The reaction mixture was left to cool, and filtered through Celite (registered trademark). The filtrate was concentrated under reduced pressure. The residue was purified by aminopropylated silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (255 mg). 1H-NMR (CDCl3) δ ppm: 3.95 (3H, s), 6.70-6.80 (1H, m), 7.13 (1H, s), 7.30-7.50 (4H, m), 7.60-7.70 (2H, m), 8.00-8.40 (1H, br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796247B2
Source datasetuspto-grants-2014_08
ORD IDord-b746733e528b4324aa072d371910b41f
Source noteuspto-grants-2014_08