HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → m-(Trifluoromethyl)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | (Trifluoromethyl)benzene | HCID 7368 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | Acetic acid nitric acid | HCID 86584207 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | m-(Trifluoromethyl)nitrobenzene | HCID 7386 | — |
Reaction Steps
The nitration step (a) may be effected by using various nitrating agents such as concentrated nitric-sulfuric acid, potassium nitrate--sulfuric acid and nitric acid-acetic acid. The preferred nitrating agent is connected nitric-sulfuric acid. The reaction is carried out by slowly adding fuming nitric acid to a mixture of benzotrifluoride in concentrated sulfuric acid while maintaining the temperature of the reaction between 0° to 40° C., preferably 20°-30° C. When the addition is complete, the reaction is allowed to continue for 1 to 2 hours, preferably 1 hour at room temperature. 3-Nitrobenzotrifluoride is isolated from the reaction mixture by conventional techniques.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831193 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-96e6305d77074995a7d9d52a6e14d2a1 |
| Source note | uspto-grants-1989_05 |