Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75507Generated: October 26, 2026

Ethyl Acetate → 3-Oxo-2-(pyridin-3-yl)butanenitrile

https://huagongshe.com/reaction/75507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant3-PyridineacetonitrileHCID 80923—
SolventTetrahydrofuranHCID 8028—
Product3-Oxo-2-(pyridin-3-yl)butanenitrileHCID 67362649—

Reaction Steps

2-(Pyridin-3-yl)acetonitrile (7.00 g, 59.3 mmol) was dissolved in THF (100 ml). NaH (60% in oil) (5.93 g, 148 mmol) was slowly added and the reaction mixture was stirred at RT for 1 hour (continuous gentle gas evolution). EtOAc (1 ml) was added and the mixture was stirred until an exothermic reaction occurred. EtOAc (7 mL) was then added slowly to maintain gentle heating. The reaction was stirred at RT for 2 hours and then approximately 75% of the THF was removed in vacuo. The resulting mixture was partitioned between Et2O and water and the aqueous phase was washed with Et2O (2×50 mL). The aqueous phase was then acidified with 1M HCl and the product was extracted into EtOAc. A significant amount of solid gradually formed between the two layers. This material was filtered off and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835444B2
Source datasetuspto-grants-2014_09
ORD IDord-3f58cba89873466883fe0c34f5a1eb50
Source noteuspto-grants-2014_09