HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Fluoro-2-(trifluoromethyl)phenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 5-Fluoro-2-(trifluoromethyl)benzyl bromide | HCID 2737578 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Fluoro-2-(trifluoromethyl)phenylacetonitrile | HCID 2737604 | — |
Reaction Steps
1.95 g (30 mmol) of potassium cyanide is added to a solution of 5.14 g (20 mmol) of 5-fluoro-2-trifluoromethylbenzyl bromide in 45 ml of ethanol/8 ml of water, and it is stirred for 64 hours at room temperature. The reaction solution is diluted with ethyl acetate and extracted with saturated sodium bicarbonate solution. The organic phase is washed with water, dried and concentrated by evaporation. The remaining residue is purified by bulb tube distillation and recrystallized. Yield: 3.6 g (89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07129270B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-0ba409e413604d19aff172b009b4e436 |
| Source note | uspto-grants-2006_10 |