Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707892Generated: October 26, 2026

Hydrochloric Acid → 2-Fluoro-4-[2-(4-propylphenyl)ethynyl]bromobenzene

https://huagongshe.com/reaction/1707892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Bromo-2-fluoro-4-iodobenzeneHCID 2725006—
Reactant1-Ethynyl-4-propylbenzeneHCID 2775133—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDiethylamineHCID 8021—
Product2-Fluoro-4-[2-(4-propylphenyl)ethynyl]bromobenzeneHCID 1936238669.6%

Reaction Conditions

Temperature5 °C

Reaction Steps

1-Bromo-2-fluoro-4-iodobenzene (15 g) was dissolved in diethylamine (17 ml) under nitrogen atmosphere, and then bis(triphenylphosphine) palladium(II) chloride (0.12 g) and copper(I) iodide (0.12 g) were added thereto, followed by stirring. The flask was cooled to 5° C. or lower, and then 4-propylphenylacetylene (8 g) was added dropwise thereto. After stirring at room temperature for 5 hours, the reaction solution was poured into a mixture of concentrated hydrochloric acid (10 ml) and ice (50 g). After extraction with chloroform, the resultant was washed with water twice, followed by distilling off chloroform. The residue was recrystallized from a mixed solvent of acetone and methanol to give 4-bromo-3-fluoro-4'-propyltolane (11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356558
Source datasetuspto-grants-1994_10
ORD IDord-781a226be4b644f1a899c8ab3adbf9c8
Source noteuspto-grants-1994_10