HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 2-(6-(2,2,2-Trifluoroethoxy)pyridin-2-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Chloromethyl)-6-(2,2,2-trifluoroethoxy)pyridine | HCID 62238846 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(6-(2,2,2-Trifluoroethoxy)pyridin-2-yl)acetonitrile | HCID 89874414 | 69% |
Reaction Steps
Sodium cyanide (0.823 g, 16.8 mmol) is added to a solution of 2-(chloromethyl)-6-(2,2,2-trifluoroethoxy)pyridine (2.0 g, 7.63 mmol, Step-4) in DMSO (38 mL) and stirred at rt for 20 hours. The reaction mixture is poured into saturated aqueous sodium hydrogen carbonate (60 mL) and extracted with EtOAc (100 mL). The organic layer is washed with water (50 mL×2) and dried over sodium sulfate. After filtration, the filtrate is concentrated in vacuo. The residue is purified by column chromatography on amine gel eluting with n-hexane/EtOAc (3:1) to give 1.13 g (69% yield) of the title compound as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187475B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-7ff6af3b9e024262be7e0c9528044d8c |
| Source note | uspto-grants-2015_11 |