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alpha-Chloro-o-xylene → 3-[(2-Methylphenyl)methoxy]pyridin-2-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | alpha-Chloro-o-xylene | HCID 11093 | — |
| 反応物 | 2-Amino-3-Hydroxypyridine | HCID 28114 | — |
| 触媒 | Trioctylmethylammonium chloride | HCID 21218 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Sodium Hydroxide | HCID 14798 | — |
| 生成物 | 3-[(2-Methylphenyl)methoxy]pyridin-2-amine | HCID 13825882 | — |
反応手順
To a mixture of 2-amino-3-hydroxypyridine (7 g) and Adogen 464 (Trademark: prepared by Aldrich Chemical Co.) (0.4 g) in 40% aqueous sodium hydroxide (32 ml) and methylene chloride (32 ml) was added 2-methylbenzyl chloride (8.42 ml) at ambient temperature. After being stirred for 24 hours, the organic layer was separated and the aqueous layer was extracted with methylene chloride. The combined extracts were washed with saturated sodium chloride aqueous solution, dried over magnesium sulfate, and evaporated in vacuo. The crystalline residue was recrystallized from ethyl acetate to give 2-amino-3-(2-methylbenzyloxy)pyridine (7.56 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04725601 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-4a0ab28d099d4c989edf76e5c61389c1 |
| 出典メモ | uspto-grants-1988_02 |