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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257885Generated: October 27, 2026

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

https://huagongshe.com/reaction/1257885

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 numberUS08461330B2
Source datasetuspto-grants-2013_06
ORD IDord-a07c6f2c8c254e21af3c0fbc3be368fc
Source noteuspto-grants-2013_06