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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 389177생성일: 2026년 10월 26일

4-Penten-1-OL → Ethyl (2S)-2-{[(pent-4-en-1-yloxy)carbonyl]amino}non-8-enoate

https://huagongshe.com/reaction/389177

반응식

참여 물질

역할이름HCID투입량
반응물4-Penten-1-OLHCID 13181—
반응물Sodium HydroxideHCID 14798—
반응물DiisopropylethylamineHCID 81531—
반응물TriphosgeneHCID 94429—
반응물ethyl (2S)-2-aminonon-8-enoateHCID 59493566—
용매1,4-DioxaneHCID 31275—
생성물Ethyl (2S)-2-{[(pent-4-en-1-yloxy)carbonyl]amino}non-8-enoateHCID 86647499122.3%

반응 단계

To a stirred solution of pent-4-en-1-ol (0.62 g, 7.21 mmol) and DIPEA (1.26 mL, 7.21 mmol) in anhydrous 1,4-dioxane (20 ml), at 10° C. and under nitrogen, was slowly added a solution of triphosgene (0.75 g, 2.52 mmol) in anhydrous 1,4-dioxane (20 mL). The reaction mixture was stirred at RT for 1 hour, and ethyl (2S)-2-aminonon-8-enoate*HCl (0.85 g, 3.61 mmol) and 1 M aqueous NaOH (7.21 ml, 7.21 mmol) added, and the reaction mixture was heated to 50° C. for 15 hours. After cooling to RT, the reaction mixture was basified to pH 8 with 1M aqueous NaOH and extracted with ether (3×200 ml). The combined organic phases were washed with water (100 mL), brine (50 mL), dried over Na2SO4, filtered and concentrated. The residue was chromatographed on silica gel (5 to 75% EtOAc in hexane) to give the title compound (0.96 g). LRMS (ESI) m/z 312.5 [(M+H)+; calcd for C17H30NO4: 312.2].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08377874B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-9b3472f1b54542038d9f5857c636b3fe
출처 메모uspto-grants-2013_02