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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518196Generated: November 3, 2026

Stannous Chloride → (5-Aminopyridin-2-yl)acetonitrile

https://huagongshe.com/reaction/1518196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
Reactant5-NITRO-2-PYRIDINEACETONITRILEHCID 12014965—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product(5-Aminopyridin-2-yl)acetonitrileHCID 2187620074%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232426B2
Source datasetuspto-grants-2012_07
ORD IDord-0057e543d848448d86e6ee868629b03f
Source noteuspto-grants-2012_07