関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 1-Bromo-3,5-dinitrobenzene | HCID 44534 | — |
| 反応物 | 2-Cyclopropyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione | HCID 44138342 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | HCID 53742787 | HCID 53742787 | 64% |
反応手順
In a 250 mL round bottom flask to a solution of 3-bromo 1,5-dinitrobenzene (2.1 g, 8.50 mmol) in toluene (90 mL) tricyclohexylphosphine (0.72 g, 2.55 mmol), Cs2CO3 (16.58 g, 51 mmol), cyclopropylboronic acid MIDA ester (2.35 g, 11.90 mmol) and 10 ml de-ionized water were added and the solution was degassed with nitrogen for 30 minutes. To the above solution Pd (OAc)2 (0.29 g, 1.28 mmol) was added under nitrogen and the reaction mixture was refluxed for 12 hours. LC MS analysis of the crude reaction indicated the completion of the reaction. The crude reaction mixture was filtered on celite pad and the volatiles were removed under reduced pressure. The dark brown oil was worked-up with 2×100 mL ethyl acetate and water (100 mL), dried on MgSO4 and ethyl acetate was evaporated under reduced pressure. The crude reaction mixture was separated by column chromatography to give Compound 8 in 64% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08377924B2 |
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| 出典データセット | uspto-grants-2013_02 |
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| ORD ID | ord-d20d963b4e424415bca180fc99270348 |
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| 出典メモ | uspto-grants-2013_02 |
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