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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920119Generated: October 30, 2026

Triethylamine → HCID 67497910, compound

https://huagongshe.com/reaction/1920119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 67498142HCID 67498142—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67497910HCID 67497910—

Reaction Conditions

Temperature66 °C

Reaction Steps

After charging 4.6 parts of 1-phenyl-3,5-di(4-bromophenyl)pyrazoline synthesized by a known method, 2.4 parts of trimethylsilylacetylene, 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 stirred at 66° C. for 8 hours and then the reaction mixture was filtered and washed with THF. The obtained filtrate was concentrated, and the precipitate was filtered, washed, recrystallized from methanol and dried at 60° C. to obtain 4.4 parts of 1-phenyl-3,5-di(4-trimethylsilylethynylphenyl)pyrazoline having a melting point of 108-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168796B2
Source datasetuspto-grants-2012_05
ORD IDord-3e28aefd8ca748a89f7195588923ef62
Source noteuspto-grants-2012_05