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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33864Generated: October 26, 2026

Methyl Benzoate → 4-(2-Quinolin-2-yl-ethyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/33864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl BenzoateHCID 7150—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant2-QuinolinecarboxaldehydeHCID 79619—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product4-(2-Quinolin-2-yl-ethyl)-benzoic acid methyl esterHCID 68575869—

Reaction Steps

To a solution of 4-[Triphenyl-phophanyl)-methyl]-benzoic acid methyl ester (1.87 g) in THF (16 ml) under N2 atmosphere at 0° C. was added sodium hydride (165 mg (60%)). After 30 min, quinoline-2-carbaldehyde (0.50 g) was added and the reaction stirred at ambient temperature for 2 h. The reaction mixture was quenched with brine, extracted with chloroform, dried magnesium sulfate, filtered and concentrated to provide the crude alkene. The crude product was placed on a parr shaker in ethanol (15 ml) with palladium hydroxide (200 mg) as the catalyst under 10 PSI of H2. After 40 min, the reaction mixture was filtered through celite and concentrated. Biotage MPLC chromatography eluting with 10-20% ethyl acetate/hexane provided the title compound. MS: (M+H m/z=292.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429665B2
Source datasetuspto-grants-2008_09
ORD IDord-68e438b175834339a48d1f36eaa20468
Source noteuspto-grants-2008_09