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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Iodo-4-nitrobenzene | HCID 12495 | — |
| Reactant | 1-Pentyne, 5-chloro- | HCID 84308 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-(5-Chloropent-1-yn-1-yl)-4-nitrobenzene | HCID 54771424 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08367829B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-a1619f377d3e480b98988f19557d7219 |
|---|
| Source note | uspto-grants-2013_02 |
|---|