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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408652Generated: October 29, 2026

Benzaldehyde → Benzyl-(4-chloro-2-methylquinolin-6-yl)amine

https://huagongshe.com/reaction/408652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-Chloroquinolin-6-amineHCID 68728424—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
ProductBenzyl-(4-chloro-2-methylquinolin-6-yl)amineHCID 68729251—

Reaction Steps

6-Amino-4-chloroquinoline (0.1 g; see step (ii) above), benzaldehyde (0.055 g) and sodium tnacetoxyborohydride (0.22 g) in 1,2-dichloroethane was stirred overnight. The mixture was diluted with dichloromethane and washed with water then dried (MgSO4), filtered and evaporated. The residue was purified by chromatography on silica eluting with a mixture of ethyl acetate and pentane. The desired fractions were concentrated and the sample evaporated to dryness to give the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759348B2
Source datasetuspto-grants-2014_06
ORD IDord-d4edff718eee47328fd49349f899fec7
Source noteuspto-grants-2014_06