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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166662Generated: November 4, 2026

Propargyl alcohol → 3-Hydroxy-1-[4-chloro-2-benzoylphenyl]propyne

https://huagongshe.com/reaction/2166662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantTriphenylphosphineHCID 11776—
Reactant5-Chloro-2-iodobenzophenoneHCID 12948262—
CatalystPalladium ChlorideHCID 24290—
SolventDiethylamineHCID 8021—
Product3-Hydroxy-1-[4-chloro-2-benzoylphenyl]propyneHCID 12841644—

Reaction Steps

A mixture of 0.17 g (1.0 mmole) of palladium chloride, 0.5 g (2.0 mmole) of triphenylphosphine, 0.1 g (0.5 mmole) of cuprous iodide, 15 g (43 mmole) of 5-chloro-2-iodobenzophenone and 60 ml of diethylamine was stirred at room temperature for 20 min. In one portion 6.0 g (107 mmole) of propargyl alcohol was added, and the resulting mixture was stirred for 24 hr. The solvent was removed at reduced pressure and the residue was dissolved in ether. The ether solution was washed with water, dried with anhydrous sodium sulfate, and concentrated at reduced pressure to give the product as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04388239
Source datasetuspto-grants-1983_06
ORD IDord-2218bc03aee44663897cef1ab09b7063
Source noteuspto-grants-1983_06