HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl cyanide → 2-Amino-1-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 2-Methoxy-5-ethyl-6-methylnicotinaldehyde | HCID 10261679 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Amino-1-(5-ethyl-2-methoxy-6-methylpyridin-3-yl)ethan-1-ol | HCID 10330759 | — |
Reaction Steps
A mixture of 2-methoxy-5-ethyl-6-methylnicotinaldehyde (1.05 g, 5.86 mmol) and trimethylsilyl cyanide (0.85 mL, 6.37 mmol) containing zinc iodide (10 mg) was stirred, under a nitrogen atmosphere, at ambient temperature for two hours. This liquid was diluted with anhydrous diethyl ether, filtered and then added dropwise to a suspension of lithium aluminum hydride (225 mg, 5.9 mmol) in diethyl ether (15 mL) under nitrogen. After two hours the reaction was quenched with saturated aqueous sodium sulfate, diluted with methylene chloride, filtered and the solvents evaporated to give a semi-solid. This residue was triturated with cold diethyl ether and the crystalline product was collected by filtration to yield 346 mg (28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05308854 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-989f814f22c349e0b0631f4de664ba38 |
| Source note | uspto-grants-1994_05 |