참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopentyl ether | HCID 10989 | — |
| 반응물 | 1-Bromo-1,2,2-triphenylethene | HCID 15354 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | Methanone, bis(3,5-dibromophenyl)- | HCID 11547805 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 2,3-Diphenyl-1,1-bis(3,5-dibromophenyl)-1H-indene | HCID 59306572 | 79% |
반응 단계
A mixture of bromotriphenylethylene (14.143 g, 42.19 mmol), magnesium (903 mg, 37.2 mmol) and i-pentylether (100 cm3) was heated to reflux for 1.75 h. Heating was temporarily removed and 1 (14.00 g, 28.12 mmol) was added. The mixture was heated to reflux under nitrogen for 20 h and then allowed to cool. Hexane (100 cm3) was added and the mixture was allowed to stand for 30 min. The resultant precipitate was collected and washed with hexane. The solid was mixed with dichloromethane (200 cm3) and aqueous ammonium chloride (1 M, 200 cm3) and stirred until fully dissolved. The aqueous layer was separated and extracted with dichloromethane (3×30 cm3) and the combined organic layers washed with aqueous ammonium chloride (1 M, 100 cm3) and water (100 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed. The residue was triturated with boiling ethanol, cooled and filtered to give 2 (16.34 g, 79%) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07723553B2 |
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| 출처 데이터셋 | uspto-grants-2010_05 |
|---|
| ORD ID | ord-0671fea9223642e3a68155cca5c7fa13 |
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| 출처 메모 | uspto-grants-2010_05 |
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