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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1906628생성일: 2026년 10월 27일

N-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine Benzylester → N-(1-ethoxycarbonyl-3-phenylpropyl)-L-alanine

https://huagongshe.com/reaction/1906628

반응식

참여 물질

역할이름HCID투입량
반응물N-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine BenzylesterHCID 13345971—
반응물HCID 178418361HCID 178418361—
촉매Acetic AcidHCID 176—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물N-(1-ethoxycarbonyl-3-phenylpropyl)-L-alanineHCID 13044262—

반응 단계

N-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine Benzylester (4.2 g) is dissolved in 40 ml ethanol, to which is added 630 mg 10% Pd-C and a few drops of acetic acid. Hydrogenation occurs under a 30 psi hydrogen atmosphere at room temperature overnight. The resulting mixture is filtered through celite and dried under vacuum to remove the solvent, yielding a residue. The residue is partitioned between chloroform and aqueous 5% NaHCO3, separated, and the chloroform layer further washed with aqueous 5% NaHCO3. The aqueous layers are combined, acidified to pH 3.5 with dilute HCl, extracted with chloroform or ethylacetate several times, dried over MgSO4, and placed under vacuum to evaporate the solvent and yield 2.5 g of the diastereoisomeric product, a brown sticky solid [TLC (Silica gel; CHCl3 /MeOH/HOAC=9:1:0.5); Rf=0.4].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04652668
출처 데이터셋uspto-grants-1987_03
ORD IDord-b0927fd42b5647caac7d9bc33a5eef9a
출처 메모uspto-grants-1987_03