HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → N-[4-Cyano-3-(trifluoromethyl)phenyl]-2-methyloxirane-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N-[4-Cyano-3-(trifluoromethyl)phenyl]-2-methylprop-2-enamide | HCID 11149469 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[4-Cyano-3-(trifluoromethyl)phenyl]-2-methyloxirane-2-carboxamide | HCID 10149314 | — |
Reaction Steps
10 ml of 30% aqueous hydrogen peroxide is heated to 35–40° C. 20 ml of acetic anhydride is added dropwise under cooling, so that the temperature does not exceed 40–50° C. 0.02 g of wolframic acid is added and the reaction mixture is stirred for 0.5 hours at 50–55° C. 3 grams of the amide (7) is added to the mixture portionwise and the reaction mixture is stirred for 6 hours at 50–55° C. The suspension is then cooled to 20–25° C. and poured, under stirring, into 100 ml of cold (0–5° C.) water. The suspension is stirred for 30 minutes and the solid is filtered off, washed by water and dried at 40–50° C. Yield: 2.44 g (76.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186854B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-8e9cd72ad75a494c9637ec5c7b4bc594 |
| Source note | uspto-grants-2007_03 |