HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Trifluoroiodomethane → Ethyl 3-trifluoromethyl-4-cyclohexylphenylglyoxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Trifluoroiodomethane | HCID 16843 | — |
| Edukt | Ethyl 3-bromo-4-cyclohexylphenylglyoxylate | HCID 20515211 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Ethyl 3-trifluoromethyl-4-cyclohexylphenylglyoxylate | HCID 20515217 | — |
Reaktionsbedingungen
| Temperatur | 140 °C |
|---|
Reaktionsschritte
To a solution of 0.01 moles of ethyl 3-bromo-4-cyclohexylphenylglyoxylate in 50 ml. of dimethylformamide is added 0.15 moles of trifluoromethyl iodide and 0.02 g. of copper powder. The reaction is shaken in a sealed tube for 5 hours at 140° C., cooled, and then filtered and evaporated in vacuo. 200 ml. of water is added to the residue and extracted with ether. The ether extract is dried, evaporated to dryness and distilled to obtain ethyl 3-trifluoromethyl-4-cyclohexylphenylglyoxylate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04264627 |
| Quelldatensatz | uspto-grants-1981_04 |
| ORD ID | ord-a8aa1f6348df47aeb95f2bf53c48bfcc |
| Quellennotiz | uspto-grants-1981_04 |