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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880768Generated: October 31, 2026

Acetonitrile → HCID 59570361, compound

https://huagongshe.com/reaction/1880768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 59570279HCID 59570279—
SolventTriethylamineHCID 8471—
ProductHCID 59570361HCID 59570361—

Reaction Conditions

Temperature90 °C

Reaction Steps

To 30 ml of acetonitrile were added 4 g of 4-[2,2,2-trifluoro-1-methyl-1-(trimethylsilyloxy)ethyl]pyridine=N-oxide, 4.45 ml of triethylamine, and 4.75 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 4.3 g of 4-[2,2,2-trifluoro-1-methyl-1-(trimethylsilyloxy)ethyl]pyridine-2-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318776B2
Source datasetuspto-grants-2012_11
ORD IDord-80a6dab7fbe94044ae3bd915d9f9cd53
Source noteuspto-grants-2012_11