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HRID 4291作成日:2026年10月23日

alpha-Chloro-o-xylene → 3-[(2-Methylphenyl)methoxy]pyridin-2-amine

https://huagongshe.com/ja/reaction/4291

反応式

関与物質

役割名称HCID仕込み量
反応物alpha-Chloro-o-xyleneHCID 11093—
反応物2-Amino-3-HydroxypyridineHCID 28114—
触媒Trioctylmethylammonium chlorideHCID 21218—
溶媒DichloromethaneHCID 6344—
溶媒Sodium HydroxideHCID 14798—
生成物3-[(2-Methylphenyl)methoxy]pyridin-2-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725601
出典データセットuspto-grants-1988_02
ORD IDord-4a0ab28d099d4c989edf76e5c61389c1
出典メモuspto-grants-1988_02