化工社化工社 化学情報印刷レポート · 研究参考用
Methanesulfonyl chloride → N-(3-ethynylphenyl)methanesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | Benzenamine, 3-ethynyl- | HCID 104682 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | N-(3-ethynylphenyl)methanesulfonamide | HCID 57131399 | — |
反応手順
To a solution of 3-ethynyl aniline (1.05 mL, 10.0 mmol) in pyridine (5 mL) was added methanesulfonyl chloride (857 μL, 1.10 eq.) at a temperature of 0° C. The resulting mixture was stirred overnight at room temperature and was then evaporated. The residue was treated with 2 N aq. HCl (25 mL) and subsequently extracted with ethyl acetate (2×30 mL). The combined organic layers were dried over MgSO4 and evaporated to give the desired methanesulfonamide in quantitative yield. It was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08524724B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-e04eb91ca7634a4a97f9b40e63bc61d3 |
| 出典メモ | uspto-grants-2013_09 |