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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385258Generated: October 29, 2026

1-Iodo-4-nitrobenzene → 1-(5-Chloropent-1-yn-1-yl)-4-nitrobenzene

https://huagongshe.com/reaction/385258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Iodo-4-nitrobenzeneHCID 12495—
Reactant1-Pentyne, 5-chloro-HCID 84308—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product1-(5-Chloropent-1-yn-1-yl)-4-nitrobenzeneHCID 54771424—

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 4-iodonitrobenzene (25 g, 100 mmol), dichlorobis(triphenylphosphine)palladium(II) (0.30 g, 0.43 mmol) and copper (I) iodide (0.18 g, 0.95 mmol) in tetrahydrofuran (300 mL) and triethylamine (150 mL) was degassed under Argon for 10 minutes. The mixture was then heated to 55° C. and treated with 5-chloropentyne (12 mL, 110 mmol) via syringe. After 30 minutes of stirring, additional quantities of dichlorobis(triphenylphosphine)palladium(II) (0.10 g) and 5-chloropentyne (1 mL) were added. After another 30 minutes of stirring, the mixture was allowed to cool to room temperature and then was filtered through a pad of Celite diatomaceous earth. The filtrate was concentrated to dryness under reduced pressure to provide 1-(5-chloropent-1-ynyl)-4-nitrobenzene, which was carried on without further purification. ES/MS calcd. for C11H11ClNO2+ 224.1. found m/z=224.2 (M+1-1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367829B2
Source datasetuspto-grants-2013_02
ORD IDord-a1619f377d3e480b98988f19557d7219
Source noteuspto-grants-2013_02