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HRID 1019075作成日:2026年10月26日

3'-Nitro-4'-methylacetophenone → 1-(3-Amino-4-methylphenyl)ethan-1-ol

https://huagongshe.com/reaction/1019075

反応式

関与物質

役割名称HCID仕込み量
反応物3'-Nitro-4'-methylacetophenoneHCID 79246—
反応物Sodium borohydrideHCID 4311764—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物1-(3-Amino-4-methylphenyl)ethan-1-olHCID 12051202—

反応手順

To an ice-cold solution of 4-methyl-3-nitroacetophenone (25 g, 139 mmol) in methanol (200 mL) is added sodium borohydride (6.2 g, 163 mmol) over 15 minutes. The mixture is stirred at room temperature for 1 hour, then is quenched with water. The mixture is rotary evaporated and the residue is partitioned between water and ethyl acetate. The organic layer is dried (magnesium sulfate) and rotary evaporated to afford a light brown viscous oil. The oil is diluted with ethyl acetate (200 mL), 5% palladium-on-carbon (5 g) is added and the mixture is treated with hydrogen at 40 psi for 18 hours. The mixture is then filtered on Celite and the filtrate is rotary evaporated to afford 3-(1-hydroxyethyl)-6-methylaniline as a light yellow, pasty solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06486190B1
出典データセットuspto-grants-2002_11
ORD IDord-d55df7e059594cfc98560ab9442fa27c
出典メモuspto-grants-2002_11