Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987188Generated: October 30, 2026

Ethanolamine → 2-[(3-Nitro-4-quinolinyl)amino]ethanol

https://huagongshe.com/reaction/987188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178526762HCID 178526762—
SolventDichloromethaneHCID 6344—
Product2-[(3-Nitro-4-quinolinyl)amino]ethanolHCID 1300735481.5%

Reaction Steps

Thionyl chloride (32.3 mL, 0.4338 mole) and N,N-dimethylformamide (32 mL, 0.4338 mole) were added sequentially to a suspension of 4-hydroxy-3-nitroquinoline (75 g, 0.3944 mole) in dichloromethane (750 ml). The reaction mixture was heated at reflux for about 2½ hours and then held at ambient temperature overnight. The reaction mixture was chilled in an ice bath and then a mixture of triethylamine (82.5 mL, 0.5916 moles) and ethanolamine (35.7 mL, 0.5916 mole) in dichloromethane was slowly added. The reaction mixture was heated at reflux for several hours and then an additional 0.5 equivalents of both triethylamine and ethanolamine were added. The reaction mixture was refluxed for an additional hour then held at ambient temperature overnight. The resulting solid was isolated by filtration, washed first with dichloromethane then with water, and dried to provide 75 g of 2-[(3-nitro-4-quinolinyl)amino]ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06630588B2
Source datasetuspto-grants-2003_10
ORD IDord-7123f9cf396b4ff2a6100c9efb869ef3
Source noteuspto-grants-2003_10