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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225939Generated: October 30, 2026

Bis(2-chloro-4-fluoro-5-nitrophenyl)carbonate → Bis(2-chloro-4-fluoro-5-aminophenyl)carbonate

https://huagongshe.com/reaction/2225939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-chloro-4-fluoro-5-nitrophenyl)carbonateHCID 14534132—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTolueneHCID 1140—
ProductBis(2-chloro-4-fluoro-5-aminophenyl)carbonateHCID 1576664971.9%

Reaction Steps

Bis(2-chloro-4-fluoro-5-nitrophenyl)carbonate (233 g, 0.57 mol), toluene (2300 ml) as a solvent, and 5% Pd/C (17.4 g) as a catalyst were put in a 5-liter round-bottom flask as equipped with a stirrer, and hydrogen gas was introduced thereinto with vigorously stirring. With progress of the reaction, the reaction system became exothermic. By introduction of hydrogen gas into the reaction system at such a rate that no hydrogen gas leaked out from the system, the reaction temperature was maintained to fall within the range of from 50° to 60° C. After reaction, the reaction mixture was heated (80° to 100° C.), and the used catalyst was taken out therefrom by filtration. The by-produced water was removed form the resulting filtrate, which was fully dried with anhydrous magnesium sulfate. The drying agent was taken out by filtration, and the solvent was removed by distillation under reduced pressure to obtain bis(2-chloro-4-fluoro-5-aminophenyl)carbonate (143 g, 0.41 mol) as a white solid. Yield: 71.9 %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344953
Source datasetuspto-grants-1994_09
ORD IDord-34b7f9dbf5a745f4aa811cb1ff658f36
Source noteuspto-grants-1994_09