돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6813생성일: 2026년 10월 23일

Sodium Cyanide → 2-Oxo-1,2,3,4-tetrahydroquinoline-6-carbonitrile

https://huagongshe.com/ko/reaction/6813

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CyanideHCID 8929—
반응물6-Iodo-3,4-dihydroquinolin-2(1H)-oneHCID 22018951—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
생성물2-Oxo-1,2,3,4-tetrahydroquinoline-6-carbonitrileHCID 15270576—

반응 단계

6-Iodo-3,4-dihydroquinolin-2(1H)-one (1.50 g; 5.50 mmol), sodium cyanide (0.54 g; 11.0 mmol), copper (I) iodide (0.105 g; 0.5 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.32 g; 0.3 mmol) were combined in a flask equipped with a reflux condenser. The flask was subjected to several evacuation-nitrogen purge cycles followed by the addition of acetonitrile (25 mL). The reaction was heated to reflux for 5 hours. After cooling, the reaction was diluted with ethyl acetate (200 mL), filtered through CELITE diatomaceous earth and rinsed with copious amounts of ethyl acetate. The organic solution was washed twice with brine (50 mL), dried over sodium sulfate, filtered through a fritted funnel, and the volatiles were removed under vacuum. The crude residue was crystallized from methanol, which afforded the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084156B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-dc386eeb65804bc3a3674cae524f7269
출처 메모uspto-grants-2006_08