HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous Chloride → (5-Aminopyridin-2-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 5-NITRO-2-PYRIDINEACETONITRILE | HCID 12014965 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5-Aminopyridin-2-yl)acetonitrile | HCID 21876200 | 74% |
Reaction Steps
To a mixture of (5-nitro-pyridin-2-yl)-acetonitrile (500 mg, 3.06 mmol) in concentrated aqueous HCl (3.1 ml) and ethanol (3.1 ml) at 0° C. SnCl2 (2.3 g, 10.11 mmol) was added. The mixture was allowed to come to room temperature and was stirred for 2 h. The mixture was partitioned between ethyl acetate and saturated aqueous NaHCO3. The aqueous layer was extracted three times with ethyl acetate and the combined organic layers were washed with brine, dried over MgSO4, filtered, and the solvent evaporated under reduced pressure to give the product as a brown oil (300 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232426B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-0057e543d848448d86e6ee868629b03f |
| Source note | uspto-grants-2012_07 |