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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1531913생성일: 2026년 10월 25일

5H-Dibenzo[a,d]cyclohepten-5-one → 5-(2,4-bis(1,1-dimethylethoxy)pyrimidin-5-yl)-5H-dibenzo[a,d]cyclohepten-5-ol

https://huagongshe.com/reaction/1531913

반응식

참여 물질

역할이름HCID투입량
반응물5H-Dibenzo[a,d]cyclohepten-5-oneHCID 16679—
반응물Ammonium ChlorideHCID 25517—
반응물5-Bromo-2,4-bis(1,1-dimethylethoxy)pyrimidineHCID 818851—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물5-(2,4-bis(1,1-dimethylethoxy)pyrimidin-5-yl)-5H-dibenzo[a,d]cyclohepten-5-olHCID 21250882—

반응 조건

온도-78 °C

반응 단계

To a solution of the product of step (i) (50 g) in dry tetrahydrofuran (11) at −78° C. was added n-butyllithium (69 ml of a 2.5 M solution in hexanes) dropwise. After 0.5 hours a solution of 5H-dibenzo[a,d]cyclohepten-5-one (44 g) in tetrahydrofuran (100 ml) was added. The reaction mixture was stirred at −78° C. for three hours and then allowed to warm to room temperature overnight. Saturated aqueous ammonium chloride solution (400 ml) was added and the mixture extracted with ethyl acetate. The organic solution was dried (MgSO4) and evaporated under reduced pressure to give the crude 5-[2,4-bis[1,1-dimethylethoxy]pyrimidin-5-yl]-5H-dibenzo[a,d]cyclohepten-5-ol which was used directly.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06200981B1
출처 데이터셋uspto-grants-2001_03
ORD IDord-b67e701fdc6a4dd4ae5231942ef25189
출처 메모uspto-grants-2001_03