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Hydrochloric Acid → N-(1,1,3,3-tetramethyl-butyl)-methanesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | tert-Octylamine | HCID 61017 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(1,1,3,3-tetramethyl-butyl)-methanesulfonamide | HCID 19681856 | — |
反応手順
Methanesulfonyl chloride (46 mL, 0.6 mol) in dichloromethane (100 mL) was added dropwise over 45 minutes to a solution of tert-octylamine (80 mL, 0.5 mol) and triethylamine (84 mL, 0.6 mol) in dichloromethane (400 mL) at 0° C. The mixture was stirred for a further 1 hour at room temperature then 1M HCl (1 L) was added in one portion. The mixture was extracted with dichloromethane (2×1 L). The organic solution was dried over MgSO4, filtered and concentrated in vacuo to afford N-(1,1,3,3-tetramethyl-butyl)-methanesulfonamide as a yellow oil (100.8g, 97%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07208506B2 |
| 出典データセット | uspto-grants-2007_04 |
| ORD ID | ord-ca3f3f3ce4db4450a9f2720c9c0de87e |
| 出典メモ | uspto-grants-2007_04 |