HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742429Generated: October 30, 2026
Bis(2-chloro-4-fluoro-5-nitrophenyl)carbonate → Bis(2-chloro-4-fluoro-5-aminophenyl)carbonate
https://huagongshe.com/reaction/742429
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 | 99.7% |
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 10L 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05554581 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-6147161dc49b45348c4b31288a7f0a3d |
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| Source note | uspto-grants-1996_09 |
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