HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-3,5-dinitrobenzotrifluoride → 2,6-Dinitro-4-(trifluoromethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-3,5-dinitrobenzotrifluoride | HCID 9809 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2,6-Dinitro-4-(trifluoromethyl)aniline | HCID 9936 | — |
Reaction Steps
A solution of 40.5 g. of 2,6-dinitro-4-trifluoromethyl-1-chlorobenzene in 300 ml. of benzene was mixed with 250 ml. of 14 N ammonium hydroxide. The reaction mixture was stirred at room temperature for about 1.5 hours, at which point in time another 100 ml. of 14 N ammonium hydroxide were added and the stirring was continued for an additional 2 hours. The organic layer was separated, was washed with water and was dried. Removal of the solvents in vacuo yielded 2,6-dinitro-4-trifluoromethylaniline, which melted at about 142°-144° C. after recrystallization from a hexane-benzene solvent mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04122184 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-0944b39f8647472ca008706ce5574c70 |
| Source note | uspto-grants-1978_10 |