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Dimethylformamide → (4-Bromo-3-methoxy-2naphtyl)-triphenylsilane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 2-Methoxy-3-(triphenylsilyl)naphthalene | HCID 4229060 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (4-Bromo-3-methoxy-2naphtyl)-triphenylsilane | HCID 86653240 | 96% |
反応手順
A 150 mL Schlenk flask was charged with 4.68 g of (3-methoxy-2-naphthyl)(triphenyl)silane (11.23 mmol) and 2.20 g of N-bromosuccinimide (NBS) (12.36 mmol) under argon followed by addition of 10 mL of dimethylformamide (DMF). The resultant mixture was stirred overnight at room temperature, then diluted with 500 mL of water and extracted with 3 times 50 mL of CH2Cl2. The combined organic extracts were washed with 200 mL of water, brine and dried over Na2SO4. The product was purified by passing through short column (silica) using a mixture heptane:EtOAc in a ratio of 15:1 as eluent to afford 5.28 g of product as off-white solid (10.66 mmol) with a yield of 96%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08492493B2 |
| 出典データセット | uspto-grants-2013_07 |
| ORD ID | ord-f9595f0a42424244aa290dc86e7d7ca8 |
| 出典メモ | uspto-grants-2013_07 |