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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 (2.93 g, 17.53 mmol) was taken up in POCl3 (17 mL, 182 mmol) and heated to reflux for 3 hours. The mixture was then cooled to room temperature and poured into ice-water. The resulting dark solution was neutralised with solid Na2CO3 and the products extracted into EtOAc (×3). The combined organic extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. Purification of the residue by silica gel chromatography (2-30% EtOAc-hexanes) gave methyl 6-chloro-2-methylpyridine-3-carboxylate as a pale yellow oil (A) and methyl 2-(chloromethyl)pyridine-3-carboxylate (B) as an orange oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08367706B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-284d896ff94d4878a6f9357d2bb47da7 |
| 出典メモ | uspto-grants-2013_02 |