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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(2-chloro-4-fluoro-5-nitrophenyl)carbonate | HCID 14534132 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Bis(2-chloro-4-fluoro-5-aminophenyl)carbonate | HCID 15766649 | 71.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344953 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-34b7f9dbf5a745f4aa811cb1ff658f36 |
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| Source note | uspto-grants-1994_09 |
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