化工社化工社 化学情報印刷レポート · 研究参考用
Water → 5-[2-(2-chlorophenyl)ethyl]-3,4-dihydro-2H-pyrrole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | alpha-Bromo-o-chlorotoluene | HCID 11905 | — |
| 反応物 | 1H-Pyrrole, 2,3-dihydro-1-methyl- | HCID 557463 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-[2-(2-chlorophenyl)ethyl]-3,4-dihydro-2H-pyrrole | HCID 58483971 | — |
反応手順
5.1 3 ml of 1-methylpyrroline are dissolved in 25 nil of THF and deprotonated at −78° C. for 30 minutes using 22.6 ml of BuLi (1 M in hexane). 6.5 g of 2-chlorobenzyl bromide are dissolved in 25 ml of THF and added dropwise at the temperature indicated. After 30 minutes, the mixture is allowed to warm to RT for 12 hours. For work-up, 50 ml of water are added, and the mixture is extracted to exhaustion with dichloromethane. The combined organic phases are dried over sodium sulfate, evaporated and purified by chromatography on silica gel, giving 4.5 g of 5-[2-(2-chlorophenyl)ethyl]-3,4-dihydro-2H-pyrrole as a colourless oil, which is employed in the next reaction; Rt.: 1.303 min; [M+H]+208.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08846694B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-c9f5f5ea06f24b79bc37081c1a132fe8 |
| 出典メモ | uspto-grants-2014_09 |