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Pyridine → N-(3-formylphenyl)methanesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | Benzaldehyde, 3-amino- | HCID 74366 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(3-formylphenyl)methanesulfonamide | HCID 2794787 | — |
反応手順
1.3 g (10.73 mmol) of 3-aminobenzenecarbaldehyde were initially charged in 30 ml of dichloromethane. 849 mg (10.73 mmol) of pyridine and 1.3 g (10.73 mmol) of methanesulfonyl chloride were added, and the mixture was then stirred at RT overnight. Ethyl acetate was added, and the reaction solution was washed in each case once with 1 N hydrochloric acid, water and saturated aqueous sodium bicarbonate solution. The organic phase was dried over sodium sulfate, filtered and evaporated. The residue was purified by column chromatography on silica gel 60 (mobile phase: dichloromethane/methanol 100/0→50/1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09187428B2 |
| 出典データセット | uspto-grants-2015_11 |
| ORD ID | ord-0ce1ef30f7a74835ba5753399bfa0386 |
| 出典メモ | uspto-grants-2015_11 |