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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271926생성일: 2026년 10월 26일

Water → benzyl (5S)-N,N-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-6-nitro-D-norleucinate

https://huagongshe.com/reaction/271926

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium BicarbonateHCID 516892—
반응물(2,3-Difluorophenyl)boronic acidHCID 2734333—
반응물benzyl (2R,5E)-2-[bis(tert-butoxycarbonyl)amino]-6-nitrohex-5-enoateHCID 25034374—
촉매Binap, (A+-)-HCID 634876—
용매1,4-DioxaneHCID 31275—
용매Sodium bicarbonate methylene chlorideHCID 23716255—
생성물benzyl (5S)-N,N-bis(tert-butoxycarbonyl)-5-(2,3-difluorophenyl)-6-nitro-D-norleucinateHCID 2503437587.4%

반응 단계

A solution of benzyl (2R,5E)-2-[bis(tert-butoxycarbonyl)amino]-6-nitrohex-5-enoate (34.0 g, 73.2 mmol), 2,3-difluorophenylboronic acid (28.9 g, 183.0 mmol) and water (4.62 mL, 256.2 mmol) in dioxane (240 mL) was degassed with argon for 15 min. To this solution was added sodium bicarbonate (3.08 g, 36.6 mmol), (S)-BINAP (1.28 g, 2.05 mmol) and acetylacetanotobis(ethylene)rhodium(I) (0.472 g, 1.83 mmol) . The mixture was stirred at RT for 2 min then heated to 35° C. After 4 h, 255 mg of (S)-BINAP and 94 mg of acetylacetanotobis(ethylene)rhodium(I) were added. After an additional 2 h the reaction was diluted with DCM/NaHCO3, the layers separated and the aqueous phase was backwashed with another portion of DCM. The combined organics were dried over magnesium sulfate, filtered and concentrated to give a residue that was purified by silica gel chromatography (5%→60% ethyl acetate/hexanes) to give the title compound (37.0 g, 87%) contaminated with˜5% 5R isomer. MS 379.1 (M+1-2Boc).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452903B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-8e8fd32df0cc4b23a0140659f231dbe6
출처 메모uspto-grants-2008_11