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Phenol → 4-(O-Benzylhydroxylamino)-3-methoxy-2-methylpyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phenol | HCID 996 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | O-Benzylhydroxylamine | HCID 102313 | — |
| 反応物 | 4-Chloro-3-methoxy-2-methylpyridine | HCID 10583046 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-(O-Benzylhydroxylamino)-3-methoxy-2-methylpyridine | HCID 15279358 | — |
反応手順
16 g of 4-chloro-3-methoxy-2-methylpyridine, 63 g of phenol and 40 g of O-benzylhydroxylamine are stirred at 120° C. under nitrogen for 4 hours. After cooling, the mixture is shaken with 500 ml of 2N NaOH and CH2Cl2. The aqueous phase is extracted a second time with CH2Cl2. After concentrating the combined CH2Cl2 phases, excess O-benzylhydroxylamine is distilled off in vacuo at 0.6 mm. The residue crystallizes on stirring with hexane. After filtering off with suction and washing with hexane 21.6 g=88.4% of product remain. The product is recrystallized from ethyl acetate. M.p.: 130° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05723450 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-5d39e4809233431997c0a9624f5079c5 |
| 出典メモ | uspto-grants-1998_03 |