化工社化工社 化学情報印刷レポート · 研究参考用
4-Methoxybenzenesulfonyl chloride → N1-isobutoxy-4-methoxy-1-benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | O-(2-Methylpropyl)hydroxylamine--hydrogen chloride (1/1) | HCID 12696238 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N1-isobutoxy-4-methoxy-1-benzenesulfonamide | HCID 22997112 | — |
反応手順
Isobutoxyamine hydrochloride (7.96 mmol, 1.0 g), 4-methoxybenzenesulfonyl chloride (7.24 mmol, 1.5 g), diisopropylethylamine (18.09 mmol, 3.15 mL) and anhydrous THF (15 mL) were combined under nitrogen. The reaction stirred at room temperature for 15 hours. The reaction solution was concentrated to a white solid and partitioned between ethyl acetate and 1N HCl. The organic layer was separated and washed with saturated aqueous sodium bicarbonate and brine, dried over magnesium sulfate and concentrated under vacuum to yield an off-white colored solid. Rf: 0.5 (2:1 hexanes/ethyl acetate); H1-NMR (CDCl3): δ 7.84 (2H,d), 6.99 (2H,d), 6.81 (1H,s), 3.87 (3H,s), 3.74 (2H,d), 1.90 (1H, septet), 0.86 (6H,d).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07419967B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-b2b2d00c64f042cfb5c1a112fb547c0e |
| 出典メモ | uspto-grants-2008_09 |