化工社化工社 化学情報印刷レポート · 研究参考用
4-Toluenesulfonyl chloride → 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1,3-Diiodopropane | HCID 12314 | — |
| 反応物 | 1,4,7-Triazacyclononane | HCID 188318 | — |
| 反応物 | 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane | HCID 10906262 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane | HCID 10906262 | — |
| 生成物 | HCID 17939386 | HCID 17939386 | — |
反応手順
N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) was prepared by reacting (1.1.3) with two equivalents of p-toluenesulfonyl chloride. Two equivalents of N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) hydrobromide were reacted with one equivalent of 1,3-diiodopropane in acetonitrile with excess potassium carbonate. 1,3-bis[N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane propane (1.1.21) was isolated and purified by chromatography. The p-toluene-sulfonyl groups were removed using sulfuric acid and HBr to yield the title compound (1.1.19). 1.1.22 1,4,7,10-Tetraazabicyclo[5.5.2]tetradecane
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06881732B2 |
| 出典データセット | uspto-grants-2005_04 |
| ORD ID | ord-40ea47cb16174880a641f1495dd0ae66 |
| 出典メモ | uspto-grants-2005_04 |