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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine Benzylester | HCID 13345971 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 촉매 | Palladium | HCID 23938 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-(1-ethoxycarbonyl-3-phenylpropyl)-L-alanine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04652668 |
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| 출처 데이터셋 | uspto-grants-1987_03 |
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| ORD ID | ord-b0927fd42b5647caac7d9bc33a5eef9a |
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| 출처 메모 | uspto-grants-1987_03 |
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