HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363250Generated: October 26, 2026
Nitrogen → 4-(2-Phenyleth-1-ynyl)thiophene-2-carbaldehyde
https://huagongshe.com/reaction/1363250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 4-Bromothiophene-2-carbaldehyde | HCID 87792 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | Bis(benzonitrile)palladium chloride | HCID 498840 | — |
| Solvent | Diisopropylamine | HCID 7912 | — |
| Product | 4-(2-Phenyleth-1-ynyl)thiophene-2-carbaldehyde | HCID 2737139 | 88.9% |
Reaction Steps
Under a N2 atmosphere, 4-bromothiophene-2-carbaldehyde (1.0 g, 5.2 mmol) was taken up in diisopropylamine (20 mL). TPP (549 mg, 2.1 mmol), bis(benzonitrile)palladium chloride ([Pd(PhCN)2]Cl2) (400 mg, 1.0 mmol), and copper iodide (199 mg, 1.0 mmol) were added. The mixture was degassed with N2 before phenylacetylene (1.15 mL, 10.4 mmol) was added, and the reaction was stirred at 70° C. for 16 h. The mixture was concentrated to a dark brown solid and chromatographed in 0-15% EtOAc in heptane to yield 4-(phenylethynyl)thiophene-2-carbaldehyde (981 mg, 88%). 1H NMR (400 MHz, CDCl3) δ (ppm): 9.93 (d, 1H), 7.88 (t, 1H), 7.85 (d, 1H), 7.53 (m, 2H), 7.38 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884124B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-0c28c548d6ce41eab751f5073a9f5344 |
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| Source note | uspto-grants-2011_02 |
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