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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431839Generated: October 26, 2026

Potassium Carbonate → 3-vinyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one

https://huagongshe.com/reaction/1431839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
Reactant3-Chloro-10,11-dihydro-5H-benzo(d)naphtho(2,3-b)pyran-8(9H)-oneHCID 69673366—
Catalystpalladium(II) acetateHCID 167845—
Solvent1-PropanolHCID 1031—
Product3-vinyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-oneHCID 69673250584.1%

Reaction Steps

A 3-neck oven-dried 500 mL round-bottom flask was cooled under Ar, then charged with 3-Chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (12.0 g, 42.1 mmol), potassium vinyltrifluoroborate (8.47 g, 6.32 mmol), Pd(OAc)2 (473 mg, 2.11 mmol), SPhos (1.74 g, 4.25 mmol), K2CO3 (17.5 g, 126 mmol) and anhydrous propanol (120 mL). The reaction mixture was sparged with Ar for 16 min, then heated to reflux for 5.5 h. Upon completion, the reaction mixture was cooled to RT and concentrated under reduced pressure. The crude residue was suspended in DCM, then washed with H2O and brine. The organic solution was dried over MgSO4, filtered and concentrated under reduced pressure. The resulting residue was further purified via silica plug, eluting with DCM to afford 3-vinyl-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (10.2 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940718B2
Source datasetuspto-grants-2015_01
ORD IDord-c9d708066d884e0cad856c498ab6bcc5
Source noteuspto-grants-2015_01