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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417566Generated: November 2, 2026

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

https://huagongshe.com/reaction/2417566

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 numberUS04469633
Source datasetuspto-grants-1984_09
ORD IDord-0a318b4333564776ac286fe3165a3d3f
Source noteuspto-grants-1984_09