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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029442Generated: November 1, 2026

4-(2-quinolinylmethoxy)Benzaldehyde → 4-Phenyl-1-(4-(2-quinolinylmethoxy)phenyl)butanol

https://huagongshe.com/reaction/1029442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-quinolinylmethoxy)BenzaldehydeHCID 14578960—
ReactantHCID 178418471HCID 178418471—
SolventTetrahydrofuranHCID 8028—
Product4-Phenyl-1-(4-(2-quinolinylmethoxy)phenyl)butanolHCID 10068544—

Reaction Steps

To a solution of the aldehyde from Step I, (1.34 g) in THF at 0° was added dropwise the 3-phenylpropylmagnesium bromide (1.1 mol. equiv., from above). After 30 mins, the reaction was quenched by the addition of 25% aqueous NH4OAc solution. The mixture was then extracted with ethyl acetate (×2), the organic phase was washed with brine (×2), dried and evaporated under reduced pressure. The title compound was obtained after recrystallization from ethyl acetate/hexane, m.p. 118°-119°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102881
Source datasetuspto-grants-1992_04
ORD IDord-f8e9c0338efd461ca9656e4de428a8dd
Source noteuspto-grants-1992_04