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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920121Generated: October 28, 2026

Triethylamine → HCID 87422751, compound

https://huagongshe.com/reaction/1920121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylacetyleneHCID 10821—
ReactantHCID 87422732HCID 87422732—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87422751HCID 87422751—

Reaction Steps

After charging 7.4 parts of 7-diethylamino-4-[(p-bromphenyl)]coumarin synthesized by a known method, 2.4 parts of phenylacetylene, 0.46 parts of tetrakis(triphenylphosphine)palladium(0), 0.038 parts of copper iodide and 20 ml of triethylamine in 40 ml of THF, the mixture was refluxed for 9 hours. The reaction mixture was filtered and washed with THF, and the obtained filtrate was concentrated and then diluted with water and filtered. The obtained cake was recrystallized from methanol. Upon drying under reduced pressure there was obtained 2.2 parts of 7-diethylamino-4-[4-(phenylethynyl)phenyl]coumarin having a melting point of 136-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168796B2
Source datasetuspto-grants-2012_05
ORD IDord-3cc4216e2e4d406db9bd93f1a732cd24
Source noteuspto-grants-2012_05