HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268918Generated: November 2, 2026
Triphenylphosphine → HCID 18446920, compound
https://huagongshe.com/reaction/1268918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Reactant | HCID 18446905 | HCID 18446905 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18446920 | HCID 18446920 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07199137B2 |
|---|
| Source dataset | uspto-grants-2007_04 |
|---|
| ORD ID | ord-86080194b2b74540a7ab79ab16a54e52 |
|---|
| Source note | uspto-grants-2007_04 |
|---|