HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2,6-Dinitro-4-(trifluoromethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Chloro-3,5-dinitrobenzotrifluoride | HCID 9809 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,6-Dinitro-4-(trifluoromethyl)aniline | HCID 9936 | — |
Reaction Steps
Twent-six grams (0.096m) of crude 4-chloro-3,5-dinitrobenzotrifluoride, 150 ml. of liquid ammonia and 150 ml. of 2B ethanol were heated in a sealed autoclave at 100° C. for about 4 hours. After cooling and venting, the reaction mixture was taken up in ethyl acetate. The ethyl acetate phase was washed with water. The ethyl acetate solution was dried and evaporated in vacuo to yield crude 4-amino-3,5-dinitrobenzotrifluoride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024142 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-c60c7e4201af4ff28c9f168523854eed |
| Source note | uspto-grants-1977_05 |