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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720425Generated: November 3, 2026

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

https://huagongshe.com/reaction/1720425

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 1576664999.7%

Reaction Steps

Bis (2 -chloro-4- fluoro- 5 -nitrophenyl ) carbonate (1.2 Kg, 2.9 mol), toluene (7 liters) as a solvent and 5% Pd/C (200 g) as a catalyst were placed in a 10 L three-necked flask equipped with a stirrer, and hydrogen gas was introduced while vigorously stirring. Heat generated as the reaction proceeded, and the reaction temperature was maintained at 60° to 70° C. by introducing hydrogen at such a rate that the hydrogen gas did not discharge from the system. After completion of the reaction, the reaction mixture was heated (60°-70° C.), and the catalyst was separated by filtration. The organic layer of the filtrate was separated and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration, and the solvent was distilled off under reduced pressure to obtain bis(2-chloro-4-fluoro-5-aminophenyl)carbonate as a white solid (1.01Kg, 2.89 mol, 99.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506190
Source datasetuspto-grants-1996_04
ORD IDord-c2be3e2eeef24ac392844d15ac3eb440
Source noteuspto-grants-1996_04