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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880718Generated: November 1, 2026

Acetonitrile → 6-Chloro-4-(trifluoromethyl)pyridine-2-carbonitrile

https://huagongshe.com/reaction/1880718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 19066096HCID 19066096—
SolventTriethylamineHCID 8471—
Product6-Chloro-4-(trifluoromethyl)pyridine-2-carbonitrileHCID 59570332—

Reaction Steps

To 16 ml of acetonitrile were added 1.5 g of 2-chloro-4-trifluoromethylpyridine N-oxide, 2.12 ml of triethylamine, and 2.26 g of trimethylsilyl cyanide, and the mixture was heated to reflux for 23 hours. Thereafter, the reaction solution was allowed to cool to room temperature, and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.9 g of 2-chloro-6-cyano-4-trifluoromethylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318776B2
Source datasetuspto-grants-2012_11
ORD IDord-0aac6075075942b5b0b7dcab1f80c5cc
Source noteuspto-grants-2012_11