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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420992Generated: October 30, 2026

Dimethylcarbamoyl Chloride → 4-(Tert-butyl-dimethylsilyloxyethyl)-2-cyanopyridine

https://huagongshe.com/reaction/2420992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantPotassium CarbonateHCID 11430—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-1-oxo-1lambda~5~-pyridineHCID 19757789—
SolventDichloromethaneHCID 6344—
Product4-(Tert-butyl-dimethylsilyloxyethyl)-2-cyanopyridineHCID 2232170997%

Reaction Steps

4-[2-(tert-Butyldimethylsiloxy)ethyl]pyridine-N-oxide (12.5 g, 49.3 mmol) was dissolved in dichloromethane (100 mL), then trimethylsilyl cyanide (5.31 g, 53.5 mmol) was added thereto at room temperature, and dimethylcarbamoyl chloride (5.76 g, 53.5 mmol) was added thereto over 30 minutes. Then, the mixture was stirred for 24 hours. After completion of the reaction was confirmed by thin-layer chromatography, a 10% aqueous potassium carbonate solution (150 mL) was added to the mixture, and the mixture was further stirred for 10 minutes. The reaction mixture was extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure to give 4-[2-(tert-butyldimethylsiloxy)ethyl]pyridine-2-carbonitrile (12.5 g, yield 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956060B2
Source datasetuspto-grants-2011_06
ORD IDord-383c76ab88fd44a2abaf691f9c4d88fd
Source noteuspto-grants-2011_06