HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-3,5-dinitrobenzotrifluoride → 2-Chloro-5-(trifluoromethyl)benzene-1,3-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-3,5-dinitrobenzotrifluoride | HCID 9809 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Chloro-5-(trifluoromethyl)benzene-1,3-diamine | HCID 12402994 | 95.8% |
Reaction Steps
40 g of 4-chloro-3,5-dinitro-benzotrifluoride and 47 g of toluene are placed in an agitator autoclave, and the catalyst suspension is flushed in with 4 g of water. Hydrogenation subsequently takes place at a temperature of 100° C. and at a hydrogen pressure of 5 bar. When the hydrogen uptake is complete, the autoclave is cooled and rendered inert with nitrogen. The catalyst is filtered off and washed with toluene. After working up by distillation, 29.8 g of 3,5-diamino-4-chloro-benzotrifluoride (yield 95.8% of theory) are obtained. Elementary analysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06197716B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-bd2165999a854fd481c554940a25c878 |
| Source note | uspto-grants-2001_03 |