HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896792Generated: October 31, 2026
Phenylacetylene → 5-Nitro-2-phenylbenzofuran
https://huagongshe.com/reaction/1896792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Iodo-4-nitrophenol | HCID 284949 | — |
| Reactant | L-Prolinol | HCID 640091 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Nitro-2-phenylbenzofuran | HCID 11172480 | 30% |
Reaction Steps
A solution of 2-iodo-4-nitrophenol (500 mg, 1.89 mmol), prolinol (573 mg, 5.66 mmol), palladium on carbon (60 mg, 0.06 mmol), triphenylphosphine (59.4 mg, 0.226 mmol) and copper iodide (22 mg, 0.113 mmol) in water (6 mL) was stirred for 1 h at room temperature. Ethynylbenzene (482 mg, 4.72 mmol) was slowly added, and the resulting mixture was heated at 80° C. for 3 h. After cooling, ethyl acetate was added, and the mixture was passed through a pad of Celite®. The filtrate was washed with water; the combined organic layers were dried over anhydrous MgSO4 and evaporated. The resulting material was purified by column chromatography eluting with ethyl acetate/hexanes 1:40 v/v to afford 134 mg (30%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518980B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-e8fbc4ccae0a4a47b640997407e9e41c |
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| Source note | uspto-grants-2013_08 |
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