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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251206Generated: October 25, 2026

Phosphorus oxychloride → 1-Chloro-3-(4-trifluoromethoxyphenyl)isoquinoline

https://huagongshe.com/reaction/1251206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-(4-Trifluoromethoxyphenyl)isoquinolin-1-oneHCID 22503222—
Product1-Chloro-3-(4-trifluoromethoxyphenyl)isoquinolineHCID 22502865—

Reaction Steps

The resulting 3-(4-trifluoromethoxyphenyl)isoquinolin-1-one (3.01 g) was reacted with phosphorus oxychloride (20 ml) according to the method of Example 10-2, to give 1-chloro-3-(4-trifluoromethoxyphenyl)isoquinoline, which was then reacted as it was with N-ethylpiperazine (40 ml) at 90° C. overnight. The reaction solution was evaporated, and to the resulting residue were added ethyl acetate and purified water. The ethyl acetate layer was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol system), to give 3.65 g of the free compound of the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-85eb97423aba4a1da1e34c8c940b5f41
Source noteuspto-grants-2002_01