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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 4-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-1-oxo-1lambda~5~-pyridine | HCID 19757789 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Tert-butyl-dimethylsilyloxyethyl)-2-cyanopyridine | HCID 22321709 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07956060B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-383c76ab88fd44a2abaf691f9c4d88fd |
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| Source note | uspto-grants-2011_06 |
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