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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275094Generated: October 31, 2026

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

https://huagongshe.com/reaction/275094

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 numberUS05391807
Source datasetuspto-grants-1995_02
ORD IDord-f6b0e25e9e874d97be6a88e790b4a4dd
Source noteuspto-grants-1995_02