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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587332Generated: November 3, 2026

Ethanol → 4-(Tert-butyldimethylsilyloxymethyl)pyridinecarbonitrile

https://huagongshe.com/reaction/1587332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-(tert-Butyldimethylsilanyloxymethyl)pyridine 1-oxideHCID 21781515—
SolventEthyl AcetateHCID 8857—
Product4-(Tert-butyldimethylsilyloxymethyl)pyridinecarbonitrileHCID 14541448—

Reaction Steps

A solution of 37.9 g of 4-(tert-butyl-dimethylsilyloxymethyl)-pyridine-N-oxide, 84 ml of trimethylsilyl cyanide and 44 ml triethylamine is stirred under nitrogen at reflux for 21/2 hours. Dark solution is cooled in an ice bath, then 40 ml of ethanol added followed by 500 ml of ethyl acetate. The solution is washed twice with water, dried over sodium sulfate, filtered, concentrated in vacuo and purified by flash chromatography using ethyl acetate/hexane (1:10) to yield 4-(tert-butyl-dimethylsilyloxymethyl)-2-cyanopyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217963
Source datasetuspto-grants-1993_06
ORD IDord-5dc3991acfd249bfa50d5acddf9b1052
Source noteuspto-grants-1993_06