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HRID 1059975作成日:2026年10月27日

4-(4-Methoxypyridin-2-yl)-2-nitrotoluene → 5-(4-Methoxypyridin-2-yl)-2-methylaniline

https://huagongshe.com/reaction/1059975

反応式

関与物質

役割名称HCID仕込み量
反応物4-(4-Methoxypyridin-2-yl)-2-nitrotolueneHCID 18631003—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物5-(4-Methoxypyridin-2-yl)-2-methylanilineHCID 1866763896.5%

反応手順

A suspension of 4-(4-methoxypyridin-2-yl)-2-nitrotoluene (300 mg) in tetrahydrofuran (3 ml) and ethanol (3 ml) was hydrogenated over palladium on carbon (10% w/w, 50% wet, 150 mg) under a hydrogen atmosphere for 3 hours. The catalyst was filtered off, and the filtrate was evaporated under reduced pressure to give 5-(4-methoxypyridin-2-yl)-2-methylaniline (254 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06521643B1
出典データセットuspto-grants-2003_02
ORD IDord-6ba881de2be0410e8f67d1743402cb68
出典メモuspto-grants-2003_02