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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268918Generated: November 2, 2026

Triphenylphosphine → HCID 18446920, compound

https://huagongshe.com/reaction/1268918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant5-Bromo-1-indanoneHCID 520695—
ReactantHCID 18446905HCID 18446905—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 18446920HCID 1844692055%

Reaction Conditions

Temperature100 °C

Reaction Steps

Palladium acetate (0.025 g, 0.11 mmol) and triphenylphosphine (0.06 g, 0.22 mmol) were suspended in toluene (1 ml). 5-bromoindanone (240 mg, 1.1 mmol) was then added and the mixture heated to 100° C. for 5 min. The solution was then treated with a solution of the product of Step 3 (0.6 g, 0.94 mmol) in toluene (1 ml) and stirred for 18 hours at 100° C. After cooling the solvent was removed in vacuo and the residue purified by silica gel chromatography, eluting with ethyl acetate to afford the title compound (0.25 g, 55%) as a yellow solid; MS(AP+) m/e 482 [M+H]+. Step 5: 5-(2-Phenyl-5-pyridin-4-yl-1H-imidazol-4-yl)-indan-1-one

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199137B2
Source datasetuspto-grants-2007_04
ORD IDord-86080194b2b74540a7ab79ab16a54e52
Source noteuspto-grants-2007_04