HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Amino-2-methyl-4-(2-trifluoromethylphenyl)butyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-[2-(Trifluoromethyl)phenyl]butan-2-one | HCID 11746021 | — |
| Solvent | Ammonia | HCID 222 | — |
| Product | 2-Amino-2-methyl-4-(2-trifluoromethylphenyl)butyronitrile | HCID 11218718 | — |
Reaction Steps
1.5 g of 4-(2-trifluoromethylphenyl)butan-2-one, 0.41 g of sodium cyanide and 0.56 g of ammonium chloride are dissolved in 77 ml of a 2M solution of ammonia in ethanol and the mixture is stirred at ambient temperature for 7 h. The mixture is subsequently concentrated under reduced pressure and the residue is redissolved in ethyl acetate and washed with water and three times with saturated sodium chloride solution. The organic phase is separated, dried with magnesium sulfate and evaporated under reduced pressure. After purifying the residue by flash chromatography, the title compound is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091371B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-f7bffe1edf2743528fa2a6dad5094133 |
| Source note | uspto-grants-2006_08 |