Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504641Generated: October 30, 2026

Toluene → 5-vinyl-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/1504641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-1-indanoneHCID 520695—
CatalystHCID 178418397HCID 178418397—
Product5-vinyl-2,3-dihydro-1H-inden-1-oneHCID 6717191448%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of 5-bromo-2,3-dihydro-1H-inden-1-one (5 g, 23.7 mmol) in toluene were added vinylboronic anhydride pyridine complex (8.55 g, 35.54 mmol), Pd(PPh3)4 (0.1 g, 0.094 mmol), K2CO3 (22.88 g, 165.83 mmol). The resultant reaction mixture was heated at reflux for 16 h. The reaction mixture was cooled to 25° C. and filtered, and the filtrate was concentrated under reduced pressure. The residue was diluted with EtOAc and washed with H2O and brine. The combined organic extracts were dried over anhydrous Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by flash column chromatography (SiO2, 5% EtOAc in petroleum ether) afforded the title compound as a solid (1.8 g, 48%): 1H NMR (400 MHz, CDCl3) δ 7.74 (d, J=7.2 Hz, 1H), 7.49 (br s, 1H), 7.44 (d, J=7.2 Hz, 1H), 6.82 (m, 1H), 5.90 (d, J=7.4 Hz, 1H), 5.42 (d, J=6.4 Hz, 1H), 3.20 (m, 2H), 2.70 (m, 2H); ESIMS m/z 159.06 ([M+H]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09215870B2
Source datasetuspto-grants-2015_12
ORD IDord-d0f7842cb6d841a3925125f56affb705
Source noteuspto-grants-2015_12