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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061588Generated: November 4, 2026

1,4-Dibromobenzene → 3,3'-(1,4-Phenylene)di(prop-2-yn-1-ol)

https://huagongshe.com/reaction/1061588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
ReactantPropargyl alcoholHCID 7859—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventPropylamineHCID 7852—
Product3,3'-(1,4-Phenylene)di(prop-2-yn-1-ol)HCID 1325299390.2%

Reaction Steps

A solution of 1,4-dibromobenzene (1.18 g, 5.0 mmol) in n-propylamine (15 ml) is admixed successively with Pd(Ph3P)4 (116 mg, 2%), CuI (28 mg, 3%) and propargyl alcohol (0.9 ml, 15 mmol) and stirred at RT for 1 h and then at reflux for 7 h. More Pd(Ph3P)4 (58 mg, 1%), CuI (14 mg, 1.5%) and propargyl alcohol (0.45 ml, 7.5 mmol) are then added, and the mixture is stirred at reflux for a further 8 h. After cooling, the reaction mixture is filtered off with suction over kieselguhr and the filter cake is washed with ethyl acetate (20 ml). The organic phase is concentrated under reduced pressure. Further purification is carried out by chromatography [Tol/Ac (8:2)] over a silica gel column. This gives the title compound (0.84 g) as a colorless solid. TLC, silica gel (glass plates), [toluene/acetone (8:2)], Rf=0.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960588B1
Source datasetuspto-grants-2005_11
ORD IDord-2ceb103273aa4ecea55d7e63ae17711d
Source noteuspto-grants-2005_11