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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364432Generated: October 31, 2026

3-Quinolinecarboxaldehyde → (Quinolin-3-yl)methanol

https://huagongshe.com/reaction/1364432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-QuinolinecarboxaldehydeHCID 83641—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(Quinolin-3-yl)methanolHCID 1266298386%

Reaction Steps

Sodium borohydride (240 mg, 6.4 mmol) was added in portions to a solution of 3-Quinoline-carboxaldehyde (910 mg, 5.8 mmol) in methanol at room temperature. Reaction was quenched after 3 hours stirring with 10 mls (aq) sat. NH4Cl. Mixture was extracted with ethyl acetate (3×30 ml). Combined organics were washed with brine and dried over MgSO4. Crude Quinolin-3-ylmethanol was obtained upon filtration and concentration (795 mg; 86% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888366B2
Source datasetuspto-grants-2011_02
ORD IDord-0e6ca74f431545cf9d27624309e880a1
Source noteuspto-grants-2011_02