HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642913Generated: October 27, 2026
Tetrahydrofuran → 1-bromo-4-(phenylethynyl)benzene
https://huagongshe.com/reaction/642913
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 1-Bromo-4-iodobenzene | HCID 11522 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-bromo-4-(phenylethynyl)benzene | HCID 290888 | 58.3% |
Reaction Steps
28.3 g (0.10 mol) of p-bromoiodobenzene, 10.2 g (0.10 mol) of phenylacetylene, 701 mg (1 mmol) of bis(triphenylphosphine)palladium(II)dichloride, and 190 mg (1 mmol) of copper (I) iodide were placed in a 1000-mL three-neck flask, and nitrogen substitution was carried out. Then, 350 mL of tetrahydrofuran and 18 mL of triethylamine were added thereto, and the mixture was stirred at room temperature for 12 hours. After the reaction, the reaction mixture washed with a 3% hydrochloric acid aqueous solution, and the aqueous phase was extracted with ethyl acetate. The extracted solution combined with the organic phase washed with brine and dried with magnesium sulfate. The mixture was filtered through celite, florisil, and alumina, and a solid obtained by the concentration of the filtrate was recrystallized with hexane to give 15 g of a solid that was the target substrate in the yield of 58%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696348B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-54a909303b374952a064f6f8bd93760e |
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| Source note | uspto-grants-2010_04 |
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