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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1949609생성일: 2026년 10월 25일

Pyridine → (S)-2-(benzoyloxy)-4-(benzyloxycarbonylamino)butanoic acid

https://huagongshe.com/reaction/1949609

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Benzoyl chlorideHCID 7412—
반응물(S)-2-Hydroxy-4-(((phenylmethoxy)carbonyl)amino)butyric acidHCID 2733930—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TetrahydrofuranHCID 8028—
생성물(S)-2-(benzoyloxy)-4-(benzyloxycarbonylamino)butanoic acidHCID 5850312851%

반응 단계

To a stirring solution of (S)-4-(benzyloxycarbonylamino)-2-hydroxybutanoic acid (1, 612 g, 2.41 mol) in THF (6 L) at 0° C. was added DMAP (2.4 g) and pyridine (196 mL, 2.41 mol). After stirring for 20 minutes, benzoyl chloride (280 mL) was added slowly and the reaction was allowed to stir overnight at room temperature. The resulting precipitate was filtered and the filtrate was acidified with 1 M citric acid (1 L). The organic solvent was removed by rotary evaporation and the desired product was extracted with EtOAc (2×2 L). The combined organic layers were washed with 1 M citric acid (1 L), brine (1 L) and then dried over MgSO4. Solvent removal under vacuum resulted in a viscous oil, which was purified on a 6-inch reverse-phase HPLC column to yield (S)-2-(benzoyloxy)-4-(benzyloxycarbonylamino)butanoic acid (2) as a non-flowing viscous oil (439 g, 51% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399419B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-d93126a2f8ba42a28863f775dba045ff
출처 메모uspto-grants-2013_03