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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880762Generated: October 31, 2026

Acetonitrile → HCID 59570299, compound

https://huagongshe.com/reaction/1880762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-[2,2,2-trifluoro-1-(triethylsilyloxy)ethyl]pyridine N-oxideHCID 59570378—
SolventTriethylamineHCID 8471—
ProductHCID 59570299HCID 59570299—

Reaction Conditions

Temperature90 °C

Reaction Steps

To 40 ml of acetonitrile were added 5 g of 4-[2,2,2-trifluoro-1-(triethylsilyloxy)ethyl]pyridine N-oxide, 5.26 ml of triethylamine, and 5.62 g of trimethylsilyl cyanide, and the mixture was stirred at 90° C. for 20 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 3 g of 4-[2,2,2-trifluoro-1-(triethylsilyloxy)ethyl]pyridine-2-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318776B2
Source datasetuspto-grants-2012_11
ORD IDord-f4dc8124fc2a43a18c4295c4153fa197
Source noteuspto-grants-2012_11