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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892144Generated: October 29, 2026

3-[(2-Methoxyethoxy)methoxy]benzaldehyde → 1-(2-Methoxyethoxy)-methoxy-3-(2-quinolin-2-yl-vinyl)-benzene

https://huagongshe.com/reaction/892144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(2-Methoxyethoxy)methoxy]benzaldehydeHCID 15755175—
ReactantTriphenyl[(quinolin-2-yl)methyl]phosphanium chlorideHCID 22241267—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Methoxyethoxy)-methoxy-3-(2-quinolin-2-yl-vinyl)-benzeneHCID 54407582—

Reaction Steps

To a cooled (−78° C.) suspension of triphenyl-(quinolin-2-yl-methyl)-phosphonium chloride (1.76 g, 4 mmol, example 17) in THF (24 mL) is added, dropwise, n-butyl lithium solution (1.7 mL, 2.5 M in hexanes). The resulting mixture is stirred for 30 min. then a solution of 3-[(2-methoxyethoxy)-methoxy]-benzaldehyde (756 mg, 3.6 mmol, example 8a) in THF (3 mL) is added. This mixture is stirred for 30 min then the cold bath removed and stirring continued for 2 h. The reaction mixture is then diluted with ethyl acetate, washed with sat. ammonium acetate solution and brine, dried over MgSO4 and concentrated. The residue is purified by flash chromatography (silica, 40% ethyl acetate in hexanes) to give the title compound as an oil. MS (ESI) 336 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005440B1
Source datasetuspto-grants-2006_02
ORD IDord-1f4301884b474332aafc444fae97cc31
Source noteuspto-grants-2006_02