Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353596Generated: October 25, 2026

Acetic Acid → (2-(4-((6-Quinolylamino)methyl)phenoxy)ethyl)diethylamine

https://huagongshe.com/reaction/353596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant6-AminoquinolineHCID 11373—
ReactantSodium HydroxideHCID 14798—
Reactant4-(2-(Diethylamino)-Ethoxy)-BenzaldehydeHCID 411674—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
Product(2-(4-((6-Quinolylamino)methyl)phenoxy)ethyl)diethylamineHCID 235143838.3%

Reaction Steps

To a stirred solution of 1.0 gram (0.0045 mole) of 4-(2-(diethylamino)ethoxy)benzaldehyde and 0.65 gram (0.0045 mole) of 6-aminoquinoline (available from Aldrich Chemical Company) in 25 mL of 1,2-dichloroethane (DCE, available from Aldrich Chemical Company) was added 0.3 mL (0.0045 mole) of glacial acetic acid (available from J. T. Baker Inc.) followed by 1.4 grams (0.0068 mole) of sodium triacetoxyborohydride (available from Aldrich Chemical Company). Upon completion of addition, the reaction mixture was stirred at ambient temperature for three hours. At the conclusion of this period, 50 mL of 10% aqueous sodium hydroxide was added dropwise. The resulting solution was extracted with three 25 mL portions of diethyl ether. The extracts were combined, washed with one 25 mL portion of an aqueous solution saturated with sodium chloride, dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 1.25 grams of a dark brown paste. The dark brown paste was purified by column chromatography on silica gel, yielding 0.13 gram of Compound 15. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753429B2
Source datasetuspto-grants-2004_06
ORD IDord-fcbe1e5a9d5b42bea75a6652b652f34a
Source noteuspto-grants-2004_06