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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352202Generated: October 31, 2026

Tricyclohexylphosphine → 2,3-Dihydro-5-[4-(phenylmethoxy)phenyl]-1H-inden-1-one

https://huagongshe.com/reaction/1352202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclohexylphosphineHCID 75806—
Reactant5-Bromo-1-indanoneHCID 520695—
ReactantPotassium FluorideHCID 522689—
Reactant4-Benzyloxy-phenylboronic acidHCID 2734314—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product2,3-Dihydro-5-[4-(phenylmethoxy)phenyl]-1H-inden-1-oneHCID 2110003036.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220734B2
Source datasetuspto-grants-2007_05
ORD IDord-2e24334c459c46f6a89d408fe879391b
Source noteuspto-grants-2007_05