関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 反応物 | 3-(chloromethyl)-2-ethylPyridine | HCID 19690958 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2-ethyl-3-chloromethylpyridine-N-oxide | HCID 19690998 | — |
反応手順
The 2-ethyl-3-chloromethylpyridine (2.4 g, 15.4 mmol) was dissolved in CHCl3 (100 mL) and cooled under nitrogen to 0° C. and m-chloroperbenzoic acid (55%, 4.2 g) was added in small portions. The reaction was stirred for 2 hours. The reaction was extracted twice with saturated aqueous sodium bicarbonate (100 mL). The organic phase was dried with MgSO4, filtered and the solvent was removed under reduced pressure. The residue was chromatographed on silica gel packed in 98:2 CH2Cl2 :MeOH and eluted with the same. The appropriate fractions were combined and the solvent removed under reduced pressure the give the desired 2-ethyl-3-chloromethylpyridine-N-oxide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05726172 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-50b5f885709f4236b5aee536d764bea9 |
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| 出典メモ | uspto-grants-1998_03 |
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