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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75507생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/75507

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물3-PyridineacetonitrileHCID 80923—
용매TetrahydrofuranHCID 8028—
생성물3-Oxo-2-(pyridin-3-yl)butanenitrileHCID 67362649—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835444B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3f58cba89873466883fe0c34f5a1eb50
출처 메모uspto-grants-2014_09