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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836296Generated: October 30, 2026

4-Quinolinecarboxaldehyde → 1-(Quinolin-4-yl)ethanol

https://huagongshe.com/reaction/1836296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-QuinolinecarboxaldehydeHCID 78072—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
Product1-(Quinolin-4-yl)ethanolHCID 531475564.9%

Reaction Steps

To 4-quinolinecarbaldehyde (2 g, 12.73 mmol) in 20 ml anhydrous ether, MeLi (1.4M, 10 ml, 13.9 mmol) was added dropwise over a period of five minutes at 0° C. The reaction mixture was stirred at room temperature for 3 hours. The solution was partitioned between ether (20 ml) and water (10 ml). The organic layer was dried over sodium sulfate, filtered and concentrated to give 1.43 g (59%) of the product which was then used as such for the subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777426B2
Source datasetuspto-grants-2004_08
ORD IDord-c81d0e82aa7b4805a7248e56e74689d6
Source noteuspto-grants-2004_08