化工社化工社 化学情報印刷レポート · 研究参考用
Lithium Hexamethyldisilazide → HCID 67271943、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 反応物 | 1-Chloro-2-(chloromethoxy)ethane | HCID 10290810 | — |
| 反応物 | Benzyl 4-cyanopiperidine-1-carboxylate | HCID 22028286 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | HCID 67271943 | HCID 67271943 | 86.2% |
反応手順
A solution of benzyl 4-cyanopiperidine-1-carboxylate (10.0 g, 41 mmol) and 2-chloroethyl chloromethyl ether (6.3 mL, 49.2 mmol) in THF (80 mL) was cooled to −78° C. To this solution was added drop wise LiHMDS (50 mL, 50 mmol, 1N in THF) and the resulting mixture was gradually warmed to room temp over 5 h. The reaction was quenched with water and the organic phase was washed with brine, dried (Na2SO4) and concentrated. The residue was purified by flash chromatography (1:1 EtOAc/hexane) to give the title compound as yellow oil (11.9 g, 86% yield). 1H NMR (300 MHz, CDCl3) δ: 7.33-7.31 (5H, m), 5.10 (2H, d, J=5.9 Hz), 4.21 (2H, bs), 3.79-3.76 (2H, m), 3.63-3.60 (2H, m), 3.52-3.51 (2H, m), 3.09 (2H, bs), 1.96-1.92 (2H, m), 1.55-1.51 (2H, m).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07897593B2 |
| 出典データセット | uspto-grants-2011_03 |
| ORD ID | ord-9af7343dc09e4601873c16461fc5d8db |
| 出典メモ | uspto-grants-2011_03 |