化工社化工社 化学情報印刷レポート · 研究参考用
Pyridine → 3-Bromo-1-(triisopropylsilyl)pyrrole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | N-Triisopropylsilylpyrrole | HCID 145136 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-Bromo-1-(triisopropylsilyl)pyrrole | HCID 2763302 | 90.1% |
反応手順
NBS (N-bromosuccinimide; 0.8 g, 4.5 mmol) was added to a stirred solution of N-(triisopropylsilyl)pyrrole (1.0 g, 4.5 mmol) in anhydrous THF (10 mL) at −78° C. The reaction mixture was kept at −78° C. for 1-2 h and then left to reach room temperature (ca. 1 h). Pyridine (0.1 mL) and hexane (10 mL) were added, the resulting suspension was filtered through a plug of neutral alumina, and the filtrate was evaporated in vacuum. Purification by column chromatography on silica gel (hexane/ethyl acetate=10:1) gave oil (1.22 g, 90.1% yield). 1H NMR (CDCl3) δ 6 1.08 (d, 18 H, Hz, Me), 1.42 (sept, 3 H, CH), 6.26 (dd, 1H, H-4), 6.66 (t, 1 H, H-5), 6.72 (dd, 1H, H-2). MS (M+H) m/z 302.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08378058B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-06fa717293be470eba1aa01f85853a1e |
| 出典メモ | uspto-grants-2013_02 |