돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27406생성일: 2026년 10월 24일

2-Piperidone → 1-(Tetrahydro-2-oxo-3-furyl)-2-piperidinone

https://huagongshe.com/ko/reaction/27406

반응식

참여 물질

역할이름HCID투입량
반응물2-PiperidoneHCID 12665—
반응물Sodium hydrideHCID 24758—
반응물2(3H)-Furanone, 3-bromodihydro-HCID 95463—
용매BenzeneHCID 241—
용매DimethylformamideHCID 6228—
생성물1-(Tetrahydro-2-oxo-3-furyl)-2-piperidinoneHCID 23342871107%

반응 조건

온도60 °C

반응 단계

1.25 g (0.05 mol) of sodium hydride (2.5 g of a 50% commercial suspension in paraffin, previously washed twice with benzene) are suspended in 50 ml of anhydrous N,N-dimethylformamide. A solution of 4.95 g (0.05 mol) of 2-piperidinone in 20 ml of N,N-dimethylformamide is added dropwise to the suspension. The mixture is then heated to 60° C. until no more gas is evolved, whereafter it is cooled. A solution of 8.25 g (0.05 mol) of 3-bromodihydro-2(3H)-furanone in 20 ml of anhydrous N,N-dimethylformamide is added dropwise while keeping the temperature at 5° to 10° C. The mixture is then stirred at 60° C. for 5 hours. N,N-Dimethylformamide is evaporated off under reduced pressure. The residue is taken up in chloroform and the insoluble matter filtered off on Norit. The filtrate is again evaporated and 9.8 g of a heavy syrup are obtained. Mass spectrum: M+. at 183 m/e.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04221789
출처 데이터셋uspto-grants-1980_09
ORD IDord-d71a5e4b990c4897a490adf4f3bc69d3
출처 메모uspto-grants-1980_09