化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → 1-Cinnamyl-4-(3-chloropropyl)piperazine dihydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Bromomethylstyrene | HCID 98116 | — |
| 反応物 | Bis(1-(3-chloropropyl)piperazine);hydrate;tetrahydrochloride | HCID 131714940 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-Cinnamyl-4-(3-chloropropyl)piperazine dihydrochloride | HCID 70415497 | 278.1% |
反応手順
6.0 g of cinnamyl bromide were added to a mixture of 7.4 g of 1-(3-chloropropyl)piperazine dihydrochloride hemihydrate, 6.1 g of triethylamine and 100 ml of reagent ethanol. The mixture was refluxed for 4 hours and then stirred overnight. After removal of the solvent in vacuo, water was added to the residue. The product was then extracted with ether and the extract was dried (magnesium sulfate) and concentrated. The resulting oil was chromatographed on silica gel (methylene chloride/methanol: 9/1) and precipitated with ethereal hydrochloric acid to give 7.4 g (70% of theory) of 1-cinnamyl-4-(3-chloropropyl)piperazine dihydrochloride.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04722926 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-d30d8a19d77a43a283a0480973ee3168 |
| 出典メモ | uspto-grants-1988_02 |