Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018659Generated: November 1, 2026

Propargyl alcohol → 3-(4-Chlorophenyl)prop-2-yn-1-ol

https://huagongshe.com/reaction/1018659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantHexaneHCID 8058—
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-4-iodobenzeneHCID 12510—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventChloroformHCID 6212—
Product3-(4-Chlorophenyl)prop-2-yn-1-olHCID 4111718—

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 6 g of 1-chloro-4-iodo-benzene, 1.8 ml of propargyl alcohol and 5.2 ml of triethylamine in 30 ml of chloroform is placed under a nitrogen atmosphere. 208 mg of bis(triphenylphosphine)palladium(II) dichloride and 98 mg of copper(I) iodide are added thereto. The reaction mixture is stirred for one hour at 40° C. 300 ml of hot n-hexane are then added. The n-hexane phase is decanted off. The residue is again digested with 200 ml of hot n-hexane, and the n-hexane phase is decanted off. The n-hexane phases are concentrated and the residue is subjected to flash chromatography on silica gel with ethyl acetate/n-hexane (1:4), yielding 3-(4-chloro-phenyl)-2-propyn-1-ol, which can be recrystallised from n-hexane, m.p. 78-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482859B1
Source datasetuspto-grants-2002_11
ORD IDord-e77121f440d541d483681898b006e8ff
Source noteuspto-grants-2002_11