HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-(Tert-butyldimethylsilyloxymethyl)pyridinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 4-(tert-Butyldimethylsilanyloxymethyl)pyridine 1-oxide | HCID 21781515 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(Tert-butyldimethylsilyloxymethyl)pyridinecarbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05057506 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-bba339e3f9d5416cb769d62894b30f35 |
| Source note | uspto-grants-1991_10 |