化工社化工社 化学情報印刷レポート · 研究参考用
HRID 67086作成日:2026年10月26日
1,2-Ethanediamine, 4-methylbenzenesulfonate (1:?) → 2-((3,4-Dichloroanilino)methyl)-2-imidazoline hydrochloride
https://huagongshe.com/reaction/67086
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,2-Ethanediamine, 4-methylbenzenesulfonate (1:?) | HCID 225030 | — |
| 反応物 | 3,4-Dichloroanilinoacetonitrile | HCID 12832559 | — |
| 溶媒 | 1,2-Dichlorobenzene | HCID 7239 | — |
| 生成物 | 2-((3,4-Dichloroanilino)methyl)-2-imidazoline hydrochloride | HCID 20528502 | 61.8% |
反応手順
A mixture of 30.15 g of 3,4-dichloroanilinoacetonitrile and 35.0 g of ethylenediamine p-toluenesulfonate in 110 ml of 1,2-dichlorobenzene was heated at reflux temperature under a small flow of nitrogen for 1.5 hours. The reaction mixture was then cooled and washed with water. The 1,2-dichlorobenzene was concentrated under vacuum and the remaining residue was put in solution in CH2Cl2 and shaken with dilute sodium hydroxide. The CH2Cl2 layer was separated and treated with diatomaceous earth and activated charcoal and then filtered. The filtrate was concentrated to dryness under vacuum and the black gummy residue which remained put in solution in isopropyl alcohol. Gaseous HCl was bubbled through the solution resulting in crystal formation. The mixture was cooled and filtered to obtain the product. Recrystallization from absolute ethanol gave 13.0 g of purified 2-((3,4-dichloroanilino)methyl)-2-imidazoline hydrochloride as tan crystals, m.p. 221°-223° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04344958 |
|---|
| 出典データセット | uspto-grants-1982_08 |
|---|
| ORD ID | ord-60abf03fdbeb4fea8dcda807345d0d3e |
|---|
| 出典メモ | uspto-grants-1982_08 |
|---|