Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222268Generated: November 1, 2026

Triphenylphosphine → HCID 69314044, compound

https://huagongshe.com/reaction/2222268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant117270-91-4HCID 14247119—
ReactantHCID 178528051HCID 178528051—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69314044HCID 69314044—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371767B2
Source datasetuspto-grants-2008_05
ORD IDord-78dde0ad53bc47f4989329e7237990f0
Source noteuspto-grants-2008_05