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Methanesulfonyl chloride → N-[2-bromo-5-(trifluoromethyl)phenyl]methanesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | 2-Bromo-5-(trifluoromethyl)benzenamine | HCID 67989 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | N-[2-bromo-5-(trifluoromethyl)phenyl]methanesulfonamide | HCID 59430904 | 52% |
反応手順
To a solution of 2-bromo-5-trifluoromethylaniline (3.18 g, 13.25 mmol) in pyridine (18 ml) was added methanesulfonyl chloride (1.03 ml, 13.25 mmol) and the mixture was stirred for 6 hours at room temperature. The solvent was removed in vacuo and the residue was diluted with chloroform. The organic layer was washed with water, 1N hydrochloric acid, a saturated sodium hydrogen carbonate solution and saturated brine and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by recrystallization to give the subject compound (2.18 g, 52%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07781479B2 |
| 出典データセット | uspto-grants-2010_08 |
| ORD ID | ord-5888ddb31d474185be9e29694440c5d9 |
| 出典メモ | uspto-grants-2010_08 |