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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623315Generated: October 31, 2026

Ethyl Acetate → 4-Chloro-6-(trifluoromethyl)-3-pyridineacetonitrile

https://huagongshe.com/reaction/623315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 72212581HCID 72212581—
SolventAcetonitrileHCID 6342—
Product4-Chloro-6-(trifluoromethyl)-3-pyridineacetonitrileHCID 8673254465.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

Trimethylsilylcyanid (TMSCN) (69.3 g, 0.7 mol) was added to a solution of 4-chloro-5-(chloromethyl)-2-(trifluoromethyl)pyridine (Int-13) (80 g, 0.348 mol) and Tetra-n-butylammoniumfluoride (129.5 g, 0.7 mol) in acetonitrile (1.5 L) slowly. Then the mixture was stirred at 20-30° C. for 2 hours. Thin layer chromatography (petroleum ether: EtOAc=3:1) showed all of starting material was consumed. The mixture was concentrated and the residue was purified by silica gel chromatography eluted with petroleum ether: EtOAc=20:1˜3:1 to yield [4-chloro-6-(trifluoromethyl)pyridin-3-yl]acetonitrile (Int-14) (50 g, 60% from NMR, 39% of yield) as yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301526B2
Source datasetuspto-grants-2016_04
ORD IDord-f2f344c87c9d4a30a72092f6ede91c52
Source noteuspto-grants-2016_04