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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 5H-Dibenzo[a,d]cyclohepten-5-one | HCID 16679 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 5-Bromo-2,4-bis(1,1-dimethylethoxy)pyrimidine | HCID 818851 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-(2,4-bis(1,1-dimethylethoxy)pyrimidin-5-yl)-5H-dibenzo[a,d]cyclohepten-5-ol | HCID 21250882 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06200981B1 |
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| 출처 데이터셋 | uspto-grants-2001_03 |
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| ORD ID | ord-b67e701fdc6a4dd4ae5231942ef25189 |
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| 출처 메모 | uspto-grants-2001_03 |
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