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Iodoethane → 3-Ethyl-1,1,2-trimethyl-1H-benzo(e)indol-3-ium Iodide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Iodoethane | HCID 6340 | — |
| 反応物 | 2,3,3-Trimethylbenzoindolenine | HCID 170530 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-Ethyl-1,1,2-trimethyl-1H-benzo(e)indol-3-ium Iodide | HCID 10090215 | 91.3% |
反応手順
Ethyl iodide (1.1 g, 7.2 mmol) was added to an acetonitrile solution (40 ml) of 1,1,2-trimethylbenz[e]indole (1) (1.0 g, 4.8 mmol, Daiichi Pure Chemicals Co., Ltd.), and then the mixture was heated under reflux for 2 days. The reaction mixture was concentrated under reduced pressure, and ether (80 ml) was added to the residue. The resulting solid was repeatedly washed with ether to obtain the title compound (2) as a dark violet solid (1.6 g, 91%). mp. 213-218° C. (decomposition).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06403625B1 |
| 出典データセット | uspto-grants-2002_06 |
| ORD ID | ord-9d9cbc1d84c94af69f860275d98eabac |
| 出典メモ | uspto-grants-2002_06 |