HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240763Generated: October 30, 2026
Cyclopropylacetylene → HCID 68722130, compound
https://huagongshe.com/reaction/240763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropylacetylene | HCID 138823 | — |
| Reactant | 5-Bromo-2-fluorobenzonitrile | HCID 2724900 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 68722130 | HCID 68722130 | — |
Reaction Steps
5-Bromo-2-fluorobenzonitrile (3.06 g, 15.3 mmol), dichlorobis(triphenylphosphine)palladium(II) (478 mg, 0.681 mmol), and copper(I) iodide (165 mg, 0.866 mmol) were combined in triethylamine (15 mL) under an inert atmosphere of nitrogen. Cyclopropylacetylene (1.8 mL) was added, and the mixture was heated to 60° C. until it turned to a black solid. The mixture was diluted with methylene chloride and washed with 1 N hydrochloric acid. The organic layer was absorbed on silica gel and purified by silica gel chromatography eluting with a gradient of 5-40% ethyl acetate in hexanes to afford the title compound. MS (ESI+) m/z 319.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648069B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-ab681ef165cf40578ae11bbc996f9bf1 |
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| Source note | uspto-grants-2014_02 |
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