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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255515Generated: November 1, 2026

Isobutylamine → 4-Isobutylamino-3-nitroquinoline

https://huagongshe.com/reaction/255515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
Reactant4-Chloro-3-nitroquinolineHCID 11275808—
SolventTetrahydrofuranHCID 8028—
Product4-Isobutylamino-3-nitroquinolineHCID 10999310—

Reaction Steps

To a stirred solution of 50.0 g (0.24 mole) of 4-chloro-3-nitroquinoline in 300 ml of tetrahydrofuran was added, in small portions, 52.7 g (0.72 mole) of isobutylamine. The mixture was heated at its reflux temperature for one hour and was then evaporated in vacuo. Water was added to the residue, and the solid was separated by filtration. The solid was suspended in one liter of water, and was dissolved by the gradual addition of concentrated hydrochloric acid (to pH 3 to 4) followed by filtration of the solution. The filtrate was basified (to pH 9 to 10) by the addition of concentrated ammonium hydroxide to provide bright yellow 4-(isobutylamino)-3-nitroquinoline, m.p. 119°-121° C. The structural assignment was supported by infrared spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698348
Source datasetuspto-grants-1987_10
ORD IDord-2c9e10e44a1f42c88f1009f784c75f84
Source noteuspto-grants-1987_10