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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548422Generated: October 29, 2026

3-Iodoaniline → HCID 10223619, compound

https://huagongshe.com/reaction/548422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-IodoanilineHCID 12271—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-6-nitroquinoline-3-carbonitrileHCID 11085690—
SolventEthanolHCID 702—
ProductHCID 10223619HCID 1022361982.9%

Reaction Steps

A mixture of 3.10 ml (25.7 mmol) 3-iodoaniline, 200 ml ethanol, and 5.00 g (21.4 mmol) 4-chloro-6-nitro-quinoline-3-carbonitrile was heated to reflux under N2 for 3½ hours. Cooled and made basic with a saturated sodium bicarbonate. Stripped solvents and azeotroped with ethanol. Slurried residue with hexane and collected. Air dried, washed solids with water, and dried in vacuo. Dissolved solids in 400 ml ethyl acetate, stirred with Darco, filtered and removed solvent. Dried solids in vacuo to give 7.38 g of yellow solid: mass spectrum (electrospray m/e): M+H=417.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE042376E1
Source datasetuspto-grants-2011_05
ORD IDord-6700d827dce747888f6c7c1780a86896
Source noteuspto-grants-2011_05