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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500229Generated: October 27, 2026

3-Bromo-3-buten-1-ol → γ-Methylene-6-quinolinepropanol

https://huagongshe.com/reaction/500229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-3-buten-1-olHCID 533975—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolineHCID 16217784—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Productγ-Methylene-6-quinolinepropanolHCID 67224309—

Reaction Conditions

Temperature100 °C

Reaction Steps

Palladium acetate (100 mg, 0.6 mmol) was added to a solution of 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline (8.0 g, 31 mmol) and 3-bromo-3-buten-1-ol (6.2 g, 41 mmol) in toluene (118 mL) and water (12 mL) followed by addition of 2-(dicyclohexylphosphino)-2′,6′-dimethoxy-1,1′-biphenyl (500 mg, 1 mmol). The mixture was stirred at 100° C. for 6 h. After cooling to RT, the mixture was diluted with EtOAc, washed with water and brine. The organic layers were dried over Na2SO4, filtered, and concentrated. The residue was purified by chromatography on silica gel with EtOAc in methylene chloride (0-50%) to afford the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-7486e9eaafc648298087d6777ab08a3a
Source noteuspto-grants-2010_08