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Triethylamine → 4-amino-N-(3-hydroxy-2,2-dimethyl-propyl)benzenesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Aminobenzenesulfonyl fluoride | HCID 66823 | — |
| 反応物 | 1-Propanol, 3-amino-2,2-dimethyl- | HCID 117326 | — |
| 溶媒 | 1-Butanol | HCID 263 | — |
| 生成物 | 4-amino-N-(3-hydroxy-2,2-dimethyl-propyl)benzenesulfonamide | HCID 21956210 | — |
反応手順
A mixture of sulphanilyl fluoride (1 g, 5.7 mmol), 3-amino-2,2-dimethylpropan-1-ol (884 mg, 8.6 mmol) and triethylamine (0.876 ml, 6.3 mmol) in butan-1-ol (20 ml) was heated at reflux for 24 hours. The volatiles were removed by evaporation and residue was purified by chromatography on silica gel to give the title compound. NMR: 0.72 (s, 6H), 2.52 (d, 2H), 3.08 (d, 2H), 4.40 (t, 1H), 7.19 (t, 1H), 7.60 (s, 1H), 7.64 (d, 2H), 7.96 (d, 2H), 8.40 (s, 1H), m/z 259 (MN)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06906065B2 |
| 出典データセット | uspto-grants-2005_06 |
| ORD ID | ord-d5979c57c8db493db62600cb3367f05e |
| 出典メモ | uspto-grants-2005_06 |