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Pyridine → 4-[(Chloromethyl)sulfanyl]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Chlorosuccinimide | HCID 31398 | — |
| 反応物 | 4-(Methylthio)pyridine | HCID 140938 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 4-[(Chloromethyl)sulfanyl]pyridine | HCID 13703981 | 46.5% |
反応手順
A solution of 4-methylthiopyridine (2.28 g, 18.2 mmol), N-chlorosuccinimide (3.0 g, 23 mmol) and pyridine (2.9 mL, 3.0 mmol) in benzene (40 mL) was heated at 50°-60° C. for 3 h. The mixture was allowed to cool to room temperature. The solvent was decanted and the residue was rinsed with benzene (2×10 mL). The organic phases were combined and evaporated. The residue was passed through a pad of silica gel (40 g) to give the title material (1.35 g) contaminated with the starting material. The impure product was repurified on silica gel preparative plates (eluted with CH2Cl2 /CH3CN: 1/1) to give the pure title material (926 mg, 32%) as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05116833 |
| 出典データセット | uspto-grants-1992_05 |
| ORD ID | ord-abb8f79711af4e5884a112e7965ac866 |
| 出典メモ | uspto-grants-1992_05 |