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HRID 1019075생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1019075

반응식

참여 물질

역할이름HCID투입량
반응물3'-Nitro-4'-methylacetophenoneHCID 79246—
반응물Sodium borohydrideHCID 4311764—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물1-(3-Amino-4-methylphenyl)ethan-1-olHCID 12051202—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06486190B1
출처 데이터셋uspto-grants-2002_11
ORD IDord-d55df7e059594cfc98560ab9442fa27c
출처 메모uspto-grants-2002_11