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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623962Generated: October 26, 2026

Phosphorus oxychloride → 6-Bromo-2-chloro-3-(4-chlorophenoxy)-4-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/623962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-bromo-3-(4-chlorophenoxy)-4-(trifluoromethyl)quinolin-2(1H)-oneHCID 86715448—
Product6-Bromo-2-chloro-3-(4-chlorophenoxy)-4-(trifluoromethyl)quinolineHCID 86715447—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a suspension of 6-bromo-3-(4-chlorophenoxy)-4-(trifluoromethyl)quinolin-2(1H)-one (1.08 g, 2.58 mmol, Intermediate 7, step c) in phosphoryl trichloride (7.2 mL, 77.3 mmol) was added diisopropylethylamine (1.33 mL, 7.74 mmol). The resulting mixture was heated at 120° C. for 8 hours. The solution was concentrated in vacuo at room temperature and the resulting residue was cooled to 0° C. with an ice bath. To the cold residue was added ice in small portions to quench excess phosphoryl trichloride. After cessation of bubbling, the solid suspension was diluted with dichloromethane. The organic phase was separated out, dried (MgSO4), filtered and concentrated to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303015B2
Source datasetuspto-grants-2016_04
ORD IDord-e19ffcb028144e6ca7ee9e4a144836dc
Source noteuspto-grants-2016_04