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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 735288생성일: 2026년 10월 27일

Cyclohexanone → 2-Cyclohepten-1-one

https://huagongshe.com/reaction/735288

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanoneHCID 7967—
반응물2-Cyclopenten-1-oneHCID 13588—
생성물2-Cyclohepten-1-oneHCID 70723—
생성물Cyclooctene-3-oneHCID 137176—
생성물2-CyclopentadecenoneHCID 54040345—

반응 단계

As may be seen in the table, cyclopentenone and cyclohexanone provided for modest enantiocontrol (12-15:1 endo:exo, 48-63% ee, 81% yield), while cycloheptenone (n=2), cyclooctenone (n=3), and (E) cyclopentadecene-2-one (n=10) were found to be highly enantioselective (entries 3-5, 5-18:1 endo:exo, 90-93% ee, 83-88% yield). Cyclopentenone (n=0, entry 1) and cyclohexanone (n=1, entry 2) were found to be somewhat less enantioselective.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07592463B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-0887465990e24916920d9fc6847df7fe
출처 메모uspto-grants-2009_09