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HRID 128781作成日:2026年10月26日

4-Hydroxy-3-nitrobenzaldehyde → 1-(2,2-Dimethoxyethyl)-3-amino-4-octyloxybenzene

https://huagongshe.com/reaction/128781

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydroxy-3-nitrobenzaldehydeHCID 18169—
反応物Ammonium formateHCID 2723923—
反応物1-(2,2-Dimethoxyethyl)-3-nitro-4-octyloxybenzeneHCID 19375116—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物1-(2,2-Dimethoxyethyl)-3-amino-4-octyloxybenzeneHCID 1937512298%

反応手順

By the method of example 1 above, 3-nitro-4-hydroxybenzaldehyde is converted into 1-(2,2-dimethoxyethyl)-3-nitro-4-octyloxybenzene. This material (1.83 g) is dissolved in ethanol (20 ml) and to the solution is added ammonium formate (3.5 g) and palladium black (0.30 g), and the mixture is stirred for 30 min. The mixture is filtered through diatomaceous earth and evaporated to dryness in vacuo. The residue is partitioned between water and dichloromethane, and the organic phase is dried over magnesium sulfate, filtered, and concentrated to give 1-(2,2-dimethoxyethyl)-3-amino-4-octyloxybenzene as an orange oil (1.64 g, 98%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464865
出典データセットuspto-grants-1995_11
ORD IDord-dd0c548b86e84427b7445ce0a434b603
出典メモuspto-grants-1995_11