HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → [4'-(Trifluoromethyl)[1,1'-biphenyl]-4-yl] acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 4-(Bromomethyl)-4'-(trifluoromethyl)-1,1'-biphenyl | HCID 22280165 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [4'-(Trifluoromethyl)[1,1'-biphenyl]-4-yl] acetonitrile | HCID 20099836 | 45% |
Reaction Steps
A mixture of 4′-bromomethyl-4-trifluoromethyl-biphenyl (0.797 g, 2.53 mmol) and potassium cyanide (0.181 g, 2.78 mmol) in N,N-dimethyl-formamide (6 mL) is stirred for eighty-eight hours at room temperature. The mixture is diluted with ethyl acetate and water. Organic phase is washed with water twice then brine, dried over sodium sulfate, filtered and concentrated. Column chromatography on silica gel with 0-40% ethyl acetate/hexane gradient gives 0.295 g (1.13 mmol, 45%) of title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989457B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-24f9df06f3b64fad91b1a6d2b9c4879d |
| Source note | uspto-grants-2011_08 |