HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222268Generated: November 1, 2026
Triphenylphosphine → HCID 69314044, compound
https://huagongshe.com/reaction/2222268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 117270-91-4 | HCID 14247119 | — |
| Reactant | HCID 178528051 | HCID 178528051 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69314044 | HCID 69314044 | — |
Reaction Steps
A solution of 3-iodo-1-(triisopropylsilyl)-1H-pyrrole (11.0 g, 2.87 mmol), triphenylphosphine (27 mg, 0.103 mmol), and tetrakis(triphenylphosphine)palladium(0) (80 mg, 0.069 mmol) in THF (20 mL) was degassed with Ar (g) for 15 min, then 2-bromo(pyridin-2-yl)zinc (1.5 mL of 0.5M solution, 5.74 mmol) was added and degassing continued a further 15 min. The reaction was stirred at 70° C. for 5 h and monitored by LC/MS. The reaction mixture was quenched with H2O (40 mL) then extracted with EtOAc (3×25 mL) and the combined organic extracts washed with brine. The organic phase was dried over Na2SO4, concentrated in vacuo and the crude residue was chromatographed on silica gel eluting with EtOAc:hexane (1:9) to afford 2-[1-(triisopropylsilyl)-1H-pyrrol-3-yl]pyridine as a clear oil which was used below without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371767B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-78dde0ad53bc47f4989329e7237990f0 |
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| Source note | uspto-grants-2008_05 |
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