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HRID 1648840생성일: 2026년 10월 24일

5H-Dibenzo[a,d]cyclohepten-5-one → dibenzo[a,d]cyclooctene-6,12(5H,7H)-dione

https://huagongshe.com/ko/reaction/1648840

반응식

참여 물질

역할이름HCID투입량
반응물5H-Dibenzo[a,d]cyclohepten-5-oneHCID 16679—
반응물2-Bromo-6,12-dioxo-5,6,7,12-tetrahydrodibenzo[a,d]cycloocteneHCID 15580927—
반응물2-Chloro-6,12-dioxo-5,6,7,12-tetrahydrodibenzo[a,d]cycloocteneHCID 15580928—
반응물2-Fluoro-6,12-dioxo-5,6,7,12-tetrahydrodibenzo[a,d]cycloocteneHCID 20480890—
용매1-Bromo-2-chlorobenzeneHCID 12754—
용매3-bromo-5H-dibenzo[a,d]cyclohepten-5-oneHCID 11483010—
용매3-Chloro-5H-dibenzo[A,D][7]annulen-5-oneHCID 12690610—
용매3-fluoro-5H-dibenzo[a,d]cyclohepten-5-oneHCID 15628590—
생성물dibenzo[a,d]cyclooctene-6,12(5H,7H)-dioneHCID 12552292—

반응 단계

Employing the procedure substantially as described in Example 1, Steps A through D, but substituting for the 5H-dibenzo[a,d]cyclohepten-5-one used in Step A thereof an equimolecular amount of 3-bromo-5H-dibenzo[a,d]cyclohepten-5-one, 3-chloro-5H-dibenzo[a,d]cyclohepten-5-one, or 3-fluoro-5H-dibenzo[a,d]cyclohepten-5-one, and o-chlorobromobenzene as solvent in Step B, there are produced, respectively, 2-bromo-6,12-dioxo-5,6,7,12-tetrahydrodibenzo[a,d]cyclooctene, m.p. 133°-138° C., 2-chloro-6,12-dioxo-5,6,7,12-tetrahydrodibenzo[a,d]cyclooctene, m.p. 148°-149° C., and 2-fluoro-6,12-dioxo-5,6,7,12-tetrahydrodibenzo[a,d]cyclooctene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04414154
출처 데이터셋uspto-grants-1983_11
ORD IDord-b06949016c6a4ab89e8f6bb23e25f2c2
출처 메모uspto-grants-1983_11