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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715392Generated: October 31, 2026

Sodium Cyanide → 2-(6-(2,2,2-Trifluoroethoxy)pyridin-2-yl)acetonitrile

https://huagongshe.com/reaction/715392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Chloromethyl)-6-(2,2,2-trifluoroethoxy)pyridineHCID 62238846—
SolventDimethyl SulfoxideHCID 679—
Product2-(6-(2,2,2-Trifluoroethoxy)pyridin-2-yl)acetonitrileHCID 8987441469%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187475B2
Source datasetuspto-grants-2015_11
ORD IDord-7ff6af3b9e024262be7e0c9528044d8c
Source noteuspto-grants-2015_11