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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297742Generated: October 27, 2026

4-Chloropyridine hydrochloride → 1-Amino-4-(4-pyridinyl)oxynaphthalene

https://huagongshe.com/reaction/2297742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloropyridine hydrochlorideHCID 81852—
Reactant4-Amino-1-naphthol hydrochlorideHCID 2723858—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-Amino-4-(4-pyridinyl)oxynaphthaleneHCID 2350586216.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirred mixture of 4-amino-1-naphthol hydrochloride (2.5 g, 12.8 mmol) and 4-chloropyridine hydrochloride (3.84 g, 29.2 mmol) in NMP (20 ml) was added potassium tert-butoxide (6.0 g, 53.47 mmol) slowly. The mixture was heated at 120° C. for 6 h, cooled to room temperature and diluted with water and dichloromethane. The combined organic extracts were washed with HCl (2N), saturated aqueous NaHCO3 and brine and dried (Na2SO4). Removal of the volatiles in vacuo afforded the product (0.5 g, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492393B1
Source datasetuspto-grants-2002_12
ORD IDord-22faf08b919c432daf0100b37956a1e1
Source noteuspto-grants-2002_12