HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707888Generated: October 25, 2026
Hydrochloric Acid → 4-Bromo-2-fluoro-4'-pentyltolane
https://huagongshe.com/reaction/1707888
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Bromo-2-fluoro-1-iodobenzene | HCID 2724516 | — |
| Reactant | 1-Ethynyl-4-pentylbenzene | HCID 2775131 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethylamine | HCID 8021 | — |
| Product | 4-Bromo-2-fluoro-4'-pentyltolane | HCID 67742263 | 41.3% |
Reaction Steps
4-Bromo-2-fluoro-1-iodobenzene (57 g) was dissolved in diethylamine (66 ml) under nitrogen atmosphere, and then bis(triphenylphosphine)palladium(II) chloride (0.5 g) and copper(I) iodide (0.5 g) were added thereto, followed by stirring. The flask was cooled to 5° C. or lower, and then 4-pentylphenylacetylene (36 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 (40 ml) and ice (30 g). After extraction with chloroform, the resultant was washed twice with water, followed by distilling off chloroform therefrom. The residue was distilled under reduced pressure (b.p. 205° to 210° C./3 mmHg), and then recrystallized from a mixed solvent of acetone and methanol to give 4-bromo-2-fluoro-4'-pentyltolane (27 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05356558 |
|---|
| Source dataset | uspto-grants-1994_10 |
|---|
| ORD ID | ord-d2e8bc9f38b24806bdd63c57f9dbb160 |
|---|
| Source note | uspto-grants-1994_10 |
|---|