HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tricyclohexylphosphine → 2,3-Dihydro-5-[4-(phenylmethoxy)phenyl]-1H-inden-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 4-Benzyloxy-phenylboronic acid | HCID 2734314 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2,3-Dihydro-5-[4-(phenylmethoxy)phenyl]-1H-inden-1-one | HCID 21100030 | 36.1% |
Reaction Steps
A solution of 4-benzyloxyphenyl boronic acid (0.15 g, 0.66 mmol), 5-bromo-1-indanone (0.10 g, 0.44 mmol), palladium acetate (2.0 mg, 0.009 mmol), tricyclohexylphosphine (7.0 mg, 0.018 mmol) and potassium fluoride (0.077 g, 1.32 mmol) in dioxane (2.5 mL) was stirred at 75° C. for 3 h. The reaction mixture was filtered through celite. Silica gel chromatography eluting with 25% ethyl acetate/hexane gave 0.05 g of desired product: 1H NMR (500 MHz, CDCl3) δ 7.85 (d, J=8.0 Hz, 1H), 7.68 (s, 1H), 7.62 (t, 3H), 7.51 (d, J=7.3 Hz, 2H), 7.46 (t, J=7.5 Hz, 2H), 7.38–7.42 (m, 1H), 7.13 (d, J=8.7 Hz, 2H), 5.18 (s, 2H), 3.23 (t, J=5.8 Hz, 2H), 2.78 (t, J=6.0 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220734B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-2e24334c459c46f6a89d408fe879391b |
| Source note | uspto-grants-2007_05 |