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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362012Generated: October 27, 2026

Acetic Acid → Methyl((quinolin-3-yl)methyl)amine

https://huagongshe.com/reaction/1362012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-QuinolinecarboxaldehydeHCID 83641—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMonomethylamine methanolHCID 57454252—
SolventMethanolHCID 887—
ProductMethyl((quinolin-3-yl)methyl)amineHCID 1649478148.2%

Reaction Steps

A solution of 3-quinolinecarboxaldehyde (1.5 g, 10 mmole), 2.0 M CH3NH2/MeOH (10 mL, 20 mmole), glacial AcOH (0.6 mL, 10 mmole), and NaBH3CN (0.35 g, 11 mmole) in MeOH (20 mL) was stirred at RT overnight, then was concentrated in vacuo. The residue was diluted with 5% NaOH and extracted with CH2Cl2. The combined organic extracts were washed with brine, dried over MgSO4, and concentrated. Flash chromatography on silica gel (10% MeOH/CH2Cl2) gave the title compound (0.83 g, 24%) as a slightly yellow viscous oil: MS (ES) m/e 173 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-702ffb54fec04a499db8394cc30a140c
Source noteuspto-grants-2011_02