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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68535Generated: October 26, 2026

Toluene → 4-(2-Fluoro-4-nitrophenyloxy)-6-methoxy-7-[3-(1-pyrrolidyl)propyloxy]quinoline

https://huagongshe.com/reaction/68535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2-Fluoro-4-nitrophenolHCID 9825—
Reactant4-Chloro-6-methoxy-7-[3-(1-pyrrolidyl)propyloxy]quinolineHCID 22646630—
SolventDichloromethaneHCID 6344—
Product4-(2-Fluoro-4-nitrophenyloxy)-6-methoxy-7-[3-(1-pyrrolidyl)propyloxy]quinolineHCID 86696917285.5%

Reaction Conditions

Temperature145 °C

Reaction Steps

2-fluoro-4-nitrophenol (36.73 g, 0.234 mol) was added to a dried chlorobenzene (5v/w, 250 mL). The mixture was heated to 145° C. Intermediate VII (12.5 g, 0.039 mol) was added to the reaction solution. The reaction was conducted at this temperature for 20 h. After completion of the reaction, the solvent was evaporated off to produce a grey solid. This solid was dissolved in CH2Cl2, and washed with a satureated saturated K2CO3 solution several times. The organic layer was collected. The solvent was dried off to produce a solid, which is recrystallized with ethanol to produce a yellow solid (49.16 g) in a yield of 71.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822465B2
Source datasetuspto-grants-2014_09
ORD IDord-f066b89403a94d5eaa5d9770d18a2c39
Source noteuspto-grants-2014_09