化工社化工社 化学情報印刷レポート · 研究参考用
Tert-Butylamine → N-tert-butyl-4-propylbenzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tert-Butylamine | HCID 6385 | — |
| 反応物 | 4-N-Propylbenzenesulphonyl chloride | HCID 2737222 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-tert-butyl-4-propylbenzenesulfonamide | HCID 6470063 | — |
反応手順
To a solution of 4-n-propylbenzenesulfonyl chloride (Lancaster) in anhydrous CH2Cl2 (0.5M solution) cooled to 0° C. under N2 was added t-butylamine (2.2 equiv) slowly through a dropping funnel. After complete addition, the reaction was stirred at room temperature for 12 hours. The CH2Cl2 was removed under reduced pressure, and the residue was extracted into ether and washed with 2N NaOH, H2O and brine. The organic phase was dried over anhydrous MgSO4 and concentrated in vacuo to afford the titled product; Rf =0.46 (3:1 hexane-EtOAc).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05281614 |
| 出典データセット | uspto-grants-1994_01 |
| ORD ID | ord-4baec7ebc0bb47e2930d93cda17f657e |
| 出典メモ | uspto-grants-1994_01 |