HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503586Generated: October 30, 2026
2-Bromo-3-pyridinol → 2-(Trimethylsilyl)furo[3,2-b]pyridine
https://huagongshe.com/reaction/503586
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromo-3-pyridinol | HCID 23070 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(Trimethylsilyl)furo[3,2-b]pyridine | HCID 13636539 | — |
Reaction Steps
A sealed pressure flask was charged with 2-bromopyridin-3-ol (10.0 g, 57.5 mmol), ethynyltrimethylsilane (15.9 ml, 115 mmol), copper (I) iodide (1.09 g, 5.75 mmol), bis(triphenylphosphine)palladium(II) chloride (2.02 g, 2.87 mmol) and 7.5 mL of dioxane. Ethynyltrimethylsilane (15.9 ml, 115 mmol) and TEA (40.0 ml, 287 mmol) were added, the vial was flushed with nitrogen, and the reaction was stirred at 50° C. for 18 h. The reaction was concentrated and purified via column chromatography (gradient elution 0-40% EtOAc:Hex) to afford 2-(trimethylsilyl)furo[3,2-b]pyridine as a brown oil. MS Found M+H+=192.3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776857B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-7980de27edaf44a0a2643814285dd86f |
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| Source note | uspto-grants-2010_08 |
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