関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Magnesium Bromide | HCID 82241 | — |
| 反応物 | 1H-Indene, 2-bromo- | HCID 575586 | — |
| 反応物 | 1-Bromo-3,5-di-tert-butylbenzene | HCID 620136 | — |
| 反応物 | HCID 178418306 | HCID 178418306 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-(3,5-di-t-Butylphenyl)indene | HCID 22283828 | 70% |
反応手順
1-Bromo-3,5-di-t-butylbenzene (47.2 g, 0.175 mol) was dissolved in ether (500 mL) and cooled to −70° C. t-Butyllithium (200 mL of 1.7 M solution in pentane, 0.34 mol) was added at −70° C. over a two hour period. The solution was allowed to warm to room temperature slowly. Magnesium bromide etherate (46.5 g, 0.18 mol) was added and the slurry was stirred for one hour. The mixture was then cooled to 5° C. and 2-bromoindene (34.2 g, 0.18 mol) was added. The mixture was warmed to room temperature and then refluxed for three hours. The solution was cooled to room temperature and the reaction was quenched carefully with water. The layers were separated and the organics washed with salt brine and dried over magnesium sulfate. The solvents were evaporated and the product was distilled twice and recrystallized from hexane to give 37.1 g of product (70%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06960550B2 |
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| 出典データセット | uspto-grants-2005_11 |
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| ORD ID | ord-76671ff5d64c49e3956b7af86a1f4c05 |
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| 出典メモ | uspto-grants-2005_11 |
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