HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Trifluoromethyl)aniline → Acetamide, N-(3-(trifluoromethyl)phenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | Acetamide, N-(3-(trifluoromethyl)phenyl)- | HCID 9595 | 93.3% |
Reaction Steps
To a solution of 161.0 g of α,α,α-trifluoro-m-toluidine in 500 ml of 2N hydrochloric acid, at room temperature, with vigorous agitation, is added rapidly 102.0 g of acetic anhydride. An exothermic reaction occurs and the temperature is allowed to rise spontaneously to about 50°. Subsequently, the mixture is allowed to cool to room temperature, and then cooled in ice. The crystalline solid is filtered to give 189.3 g of α,α,α-trifluoro-m-acetotoluidide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062846 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-9ba218216ca74aba96a009fcd91e9c03 |
| Source note | uspto-grants-1977_12 |