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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369444Generated: November 1, 2026

Phenylacetylene → HCID 46224400, compound

https://huagongshe.com/reaction/2369444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantHCID 69670677HCID 69670677—
CatalystCopper iodideHCID 83717—
SolventTriethylamineHCID 8471—
ProductHCID 46224400HCID 4622440096%

Reaction Steps

A suspension of PdCl2PPH3 (0.027 g, 0.063 mmol) and copper iodide (0.0035 g, 0.018 mmol) in 3 ml of triethylamine was charged into a 50-ml eggplant flask equipped with a stirrer. To this suspension, a solution of (trifluoromethyl)(2-iodophenyl)sulfide (0.57 g, 1.9 mmol) prepared in Example 1 and phenylacetylene (0.23 g, 2.2 mmol) in 2 ml of triethylamine was added dropwise at room temperature, and the mixture was stirred overnight. After completion of the reaction, a solvent was removed, water was added to the obtained residue, and the mixture was extracted three times with ether. The obtained organic layers was collected and washed with water, dried over anhydrous sodium sulfate, and concentrated to obtain a crude product. The obtained crude product was purified by silica gel column chromatography (Benzen/Hexane=20/80) to give target (trifluoromethyl)-(2-(2-phenylethynyl)phenyl)sulfide (0.5 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703969B2
Source datasetuspto-grants-2014_04
ORD IDord-393d15d1ebf24769841938714b011bcd
Source noteuspto-grants-2014_04