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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722333Generated: November 1, 2026

Hydrochloric Acid → 5-(2-Bromophenyl)-4-pentynoic acid

https://huagongshe.com/reaction/1722333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Bromo-2-iodobenzeneHCID 11415—
Reactant4-Pentynoic acidHCID 22464—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDiethylamineHCID 8021—
Product5-(2-Bromophenyl)-4-pentynoic acidHCID 14798467—

Reaction Steps

To 10 ml of diethylamine was added with stirring 0.5 g (5.1 mmol) of 4-pentynoic acid, 1.4g (5 mmol) of 1-bromo-2-iodobenzene, and 60mg (0.05 mmol) of tetrakis(triphenylphosphine)palladium(O) The slurry was degassed with argon and 0.19g (1.0 mmol) of CuI was added. The reaction mixture was stirred for 2 hr. at room temperature and then poured into approximately 100ml of a 10% HCl solution. The resulting precipitate was filtered, washed with water and dried. The solid was taken up in hot CHCl3 and filtered to remove insoluble salts. After evaporation of the solvent, the resulting orange solid was recrystallized from a chloroform-hexane mixture to produce a tan solid, m.p. 87-91°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855324
Source datasetuspto-grants-1989_08
ORD IDord-faa30264305d4ebdb1c8ba56d797c0bf
Source noteuspto-grants-1989_08