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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345348Generated: October 29, 2026

Ethanol → 4-(Tert-butyldimethylsilyloxymethyl)pyridinecarbonitrile

https://huagongshe.com/reaction/345348

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 numberUS05057506
Source datasetuspto-grants-1991_10
ORD IDord-bba339e3f9d5416cb769d62894b30f35
Source noteuspto-grants-1991_10