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m-Chloroperbenzoic acid → 3-Chloromethyl-2-methyl-pyridine 1-oxide
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-methylpyridine | HCID 12243711 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 3-Chloromethyl-2-methyl-pyridine 1-oxide | HCID 22053606 | — |
反応手順
To a stirred solution of 3-chloromethyl-2-methylpyridine from Step 2 above (0.50 g; 3.5 mmol) in CHCl3 (40 mL) was added m-chloroperoxybenzoic acid (1.1 g of 55:45 mCPBA:mCBA; 3.5 mmol). After 1.5 h, TLC analysis indicated complete conversion to a lower Rf product. The solution was extracted with equal volumes of saturated aqueous NaHCO3 and water, dried (MgSO4), filtered, and evaporated under reduced pressure. The residue was purified by pressurized silica gel column chromatography using 97:3 CH2Cl2 :MeOH as eluant. 3-Chloromethyl-2-methylpyridine N-oxide was obtained as a solid (TLC: Rf =0.30 (97:3 CH2Cl2 :MeOH); FAB MS m/z 158 (M+ +H)).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05726172 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-b8dbba8e74ff4118bc3513f530757669 |
| 出典メモ | uspto-grants-1998_03 |