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Sodium Carbonate → Methyl 2-(chloromethyl)pyridine-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | Methyl 2-methylnicotinate 1-oxide | HCID 20163965 | — |
| 生成物 | Methyl 2-(chloromethyl)pyridine-3-carboxylate | HCID 19081344 | — |
| 生成物 | Methyl 6-chloro-2-methylpyridine-3-carboxylate | HCID 59650775 | — |
反応手順
Methyl 2-methylpyridine-3-carboxylate 1-oxide (33.2 g, 199 mmol) was stirred in refluxing POCl3 (200 mL, 2146 mmol) for 3 hours. After cooling to room temperature, the reaction mixture poured into ice-water. The resulting dark solution was neutralized with solid sodium carbonate and the products extracted into ethyl acetate (3×). The combined organic extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography (silica, 2-20% ethyl acetate/hexanes) gave methyl 2-(chloromethyl)pyridine-3-carboxylate as an orange oil and methyl 6-chloro-2-methylnicotinate as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08278335B2 |
| 出典データセット | uspto-grants-2012_10 |
| ORD ID | ord-12c228aa751a4984b6a94d508ca70b5f |
| 出典メモ | uspto-grants-2012_10 |