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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36560생성일: 2026년 10월 25일

Triethylamine → (S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acid

https://huagongshe.com/reaction/36560

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Acetic acid, 2-fluoro-, 1,1'-anhydrideHCID 67886—
반응물N-(tert-butoxycarbonyl)-L-aspartic acidHCID 99718—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매BenzeneHCID 241—
생성물(S)-3-((tert-Butoxycarbonyl)amino)-5-fluoro-4-oxopentanoic acidHCID 10131156—

반응 단계

A suspension of Boc-Asp-OH (8.11 mmol) and fluoroacetic anhydride (16.2 mmol) in benzene (30 ml) was treated with triethylamine (16.2 mmol) at room temperature. The catalyst 4-dimethylaminopyridine (0.41 mmol) was added to the solution and the reaction stirred for about 2 h at room temperature. About 100 ml benzene was added to the reaction mixture. The organic solution was washed with 1N HCl (2×50 ml), saturated NaHCO3 (2×50 ml), and saturated NaCl (2×50 ml), followed by drying over anhydrous MgSO4. The solvent was then removed by evaporation under reduced pressure. The resulting oil was applied to a 2.5×80 cm column of silica gel (60-200 mesh). The title compound was eluded with 2% methanol in chloroform.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05416013
출처 데이터셋uspto-grants-1995_05
ORD IDord-1f37921e0a2e4e799336bdb217625c12
출처 메모uspto-grants-1995_05