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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663306Generated: October 28, 2026

8-Aminoquinoline → 4-Chloroquinolin-8-amine

https://huagongshe.com/reaction/1663306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-AminoquinolineHCID 11359—
ReactantChlorosuccinimideHCID 31398—
SolventIsopropanolHCID 3776—
Product4-Chloroquinolin-8-amineHCID 1260427434%

Reaction Conditions

Temperature25 °C

Reaction Steps

8-amino quinoline (4.5 g, 31.3 mmol), N-chlorosuccinimide (4.80 g, 36 mmol) was taken up in iPrOH (50 mL) at 60° C. The mixture was heated to reflux and stirred for 20 min. The solution was cooled to 25° C. and concentrated to ⅓ original volume. The mixture was partitioned between CH2Cl2 and water. The aqueous layer was extracted with CH2Cl2. The combined organic layers were dried over Na2SO4, filtered, and concentrated. The crude product was purified by flash chromatography (5:1 hexanes/EtOAc) to afford 1.90 g (34%) of a 8-amino-4-chloro-quinoline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034933B2
Source datasetuspto-grants-2011_10
ORD IDord-b7a6a4e82fbe4705bdfc9e68ad8bd688
Source noteuspto-grants-2011_10