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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6804Generated: October 25, 2026

4-Nitroaniline → 2-chloro-3-methyl-6-nitroQuinoline

https://huagongshe.com/reaction/6804

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitroanilineHCID 7475—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPropionyl chlorideHCID 62324—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product2-chloro-3-methyl-6-nitroQuinolineHCID 22019004—

Reaction Steps

To a solution of 4-nitroaniline (10 g, 72 mmol) in chloroform at 0° was added propionyl chloride (7 mL, 80 mol) followed by triethylamine (11.1 mL). The resulting solution was stirred for 2 h at r.t. at which time the reaction mixture was washed with aq. 2N HCl. The organic layer was dried filtered and the solvent removed under vacuum to provide a solid. A solution of phosphorous oxychloride (25 mL) and N,N-dimethylformamide (4.5 mL) was stirred at 0° for 0.15 h then the above solid was added. The resulting reaction mixture was heated at 75° for 12 h at which time the volatiles were removed under vacuum. The residue was cooled in an ice bath. To the cooled mixture was carefully added water (50 mL). The resulting solids were filtered and then washed with water. The solids were extracted with chloroform, the extracts were combined, dried, filtered and the solvent removed under vacuum to afford the product, MS: m/z 224 (MH+), which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084156B2
Source datasetuspto-grants-2006_08
ORD IDord-5d813e8fedc748868d00c8e9808dda4f
Source noteuspto-grants-2006_08