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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 981371생성일: 2026년 10월 25일

Formic Acid → (1S,2R)-2-amino-1-phenylpropan-1-ol

https://huagongshe.com/reaction/981371

반응식

참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물(1R,2S)-1-phenyl-2-(N,N-dibenzylamino)-1-propanolHCID 12105160—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물(1S,2R)-2-amino-1-phenylpropan-1-olHCID 26934—

반응 단계

To remove the benzyl group, 3.9 mmol of (1R,2S)-1-phenyl-2-(N,N-dibenzylamino)-1-propanol are dissolved in 5 ml of methanol. This solution is added to a mixture of 40 ml of methanol, 10.6 g of formic acid and 50 mg of palladium black. The air is displaced from the reaction vessel using hydrogen. After hydrogenation for 1 hour, the palladium catalyst is filtered off, and the solution is concentrated in vacuo. The residue is taken up in 10 ml of methanol and stirred with 1 g of silica gel and 5 drops of concentrated hydrochloric acid at room temperature for 1 hour. The residue obtained after removal of the silica gel by filtration and concentration of the filtrate is purified by chromatography. 243 mg (=60% of theory) of analytically pure norephedrine are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04990669
출처 데이터셋uspto-grants-1991_02
ORD IDord-4dffb0f709fb45c9ae0eaf63e77339f3
출처 메모uspto-grants-1991_02