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Tert-Butylamine → N-(1,1-Dimethylethyl)benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tert-Butylamine | HCID 6385 | — |
| 反応物 | Benzenesulfonyl chloride | HCID 7369 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-(1,1-Dimethylethyl)benzenesulfonamide | HCID 314059 | 95.6% |
反応手順
To a cooled (0° C.) solution of tert-butylamine (42.9 mL, 410.6 mmol) in THF (840 mL) was added dropwise benzenesulfonyl chloride (26.2 mL, 205 mmol) and the reaction mixture was stirred at room temperature under an argon atmosphere for 6 h. The mixture was then filtered and the collected solid washed with THF. The filtrate was concentrated, redissolved in CH2Cl2 and washed with 0.1N HCl and H2O. The organic solution was dried and concentrated to afford the desired product (41.8 g, 95%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05827863 |
| 出典データセット | uspto-grants-1998_10 |
| ORD ID | ord-1b6044d52b904ce0a18f29ce5dce3756 |
| 出典メモ | uspto-grants-1998_10 |