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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198876Generated: November 1, 2026

Acetic Acid → 4-(Hydroxymethyl)quinoline

https://huagongshe.com/reaction/1198876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
Reactant4-QuinolinecarboxaldehydeHCID 78072—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product4-(Hydroxymethyl)quinolineHCID 80479—

Reaction Steps

To a stirred solution of 10 g of 4-quinolinecarboxaldehyde in 400 ml of absolute ethanol at room temperature is added 2.4 g of sodium borohydride. After 45 minutes, 20 ml of water is added and the reaction mixture is stirred for an additional 20 minutes. Acetic acid (20 ml) is added slowly. The reaction mixture is evaporated to a small volume and partitioned between water and methylene chloride. The organic layer is washed with saturated potassium carbonate, saturated sodium chloride solution, dried over sodium sulfate and evaporated to dryness. The residue is purified by chromatography on silica gel using methanol/methylene chloride (1:10) as eluent to yield 4-hydroxymethylquinoline; Rf =0.59.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898854
Source datasetuspto-grants-1990_02
ORD IDord-cfd04df02d6d457dbe5ad093dc675f4a
Source noteuspto-grants-1990_02