HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Nitrite → 2'-Bromo-6'-trifluoromethylacetanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Nitrite | HCID 8026 | — |
| Reactant | 4'-Amino-2'-bromo-6'-trifluoromethylacetanilide sulfate | HCID 68143031 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2'-Bromo-6'-trifluoromethylacetanilide | HCID 23253853 | — |
Reaction Steps
To a suspension of 4'-amino-2'-bromo-6'-trifluoromethylacetanilide sulfate is added two molar equivalents of ethyl nitrite. The reaction mixture is cooled (0°) and stirred for 2 hours then allowed to warm to 25° and a catalytic amount of copper bronze is added. The mixture is stirred for 3 hours with the temperature maintained below 40°. The mixture is then refluxed briefly and cooled. Addition of water gives 2'-bromo-6'-trifluoromethylacetanilide which is collected by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976633 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-dd4655ba82d6419181b51500ae1e787d |
| Source note | uspto-grants-1976_08 |