Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132990생성일: 2026년 10월 25일
Potassium Iodide → (4-Iodo-5-oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-1-yl)methyl acetate
https://huagongshe.com/reaction/132990
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Thallium(1+);2,2,2-trifluoroacetate | HCID 21902506 | — |
| 반응물 | (5-Oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-1-yl)methyl acetate | HCID 58646841 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Trifluoroacetic acid | HCID 6422 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (4-Iodo-5-oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-1-yl)methyl acetate | HCID 12150904 | — |
반응 단계
4.4 g of (5-oxo-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-1-yl)methyl acetate prepared in Example 1-f was dissolved in 30 ml of trifluoroacetic acid, and 5.0 g of thallium trifluoroacetate was added at room temperature in an atmosphere of nitrogen gas. The mixture was stirred at room temperature for 4 hours, followed by stirring at 50° C. for 2 hours. After the starting material disappeared, 3 ml of an aqueous solution of 1.5 g of potassium iodide was added to the reaction mixture and the mixture was stirred at room temperature for 0.5 hour. To the reaction mixture were added ethyl acetate and water, and the mixture was neutralized with sodium hydrogencarbonate and filtered through Celite. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified and separated by silica gel column chromatography (ethyl acetate:hexane=1:20), to give 4.1 g of a 3:1 mixture of the title compounds as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07390797B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-beb1bafe3a1c4769af44e738bbebdf18 |
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| 출처 메모 | uspto-grants-2008_06 |
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