HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(4-Chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(4-Chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionitrile | HCID 13384298 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionamide | HCID 13384299 | — |
Reaction Steps
A mixture of 2-(4-chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionitrile (20 g.), potassium hydroxide (25 g.), ethanol (250 ml.) and water (250 ml.) is heated under reflux for 15 minutes. Most of the ethanol is evaporated in vacuo, and the residue is cooled until the precipitated oil solidifies. The solid is filtered off, and is recrystallised from a mixture of ether and light petroleum (b.p. 40°-60° C.) (charcoal) to give 2-(4-chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionamide, m.p. 94°-95° C. (13.9 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055595 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-fe8f915bc1f54480986a27178c9246ce |
| Source note | uspto-grants-1977_10 |