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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1070382생성일: 2026년 10월 26일

Furan → (3,5-Dioxo-10-oxa-4-azatricyclo[5.2.1.02,6]dec-4-yl)acetonitrile

https://huagongshe.com/reaction/1070382

반응식

참여 물질

역할이름HCID투입량
반응물FuranHCID 8029—
반응물MaleimideHCID 10935—
반응물BromoacetonitrileHCID 11534—
반응물10-Oxa-4-azatricyclo(5.2.1.02,6)decane-3,5-dioneHCID 239727—
용매AcetoneHCID 180—
용매DimethylformamideHCID 6228—
생성물(3,5-Dioxo-10-oxa-4-azatricyclo[5.2.1.02,6]dec-4-yl)acetonitrileHCID 22396537—

반응 단계

Synthesis took place in analogy to Example VI a from 10-oxa-4-azatricyclo[5.2.1.02,6]decane-3,5-dione (obtainable from maleimide and furan from Diels-Alder reaction for example as described by Padwa, A.; Dimitroff, M.; Waterson, A. G.; Wu, T.; J Org Chem 1997, 62, 4088-4096 and subsequent hydrogenation as described by Ansell, M. F.; Caton, M. P. L.; North, P. C.; Tetrahedron Lett. 1982, 23, 2811) and bromoacetonitrile with the exception that acetone was used as solvent in place of DMF. The substance was employed as crude product in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06903089B1
출처 데이터셋uspto-grants-2005_06
ORD IDord-5397b9d01bdc473a8cd5f7b98554a071
출처 메모uspto-grants-2005_06