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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32837생성일: 2026년 10월 24일

Acetic Acid → (S)-3-((2S,3R)-2-azido-3-phenyl-butyryl)-4-phenyl-oxazolidin-2-one

https://huagongshe.com/ko/reaction/32837

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2,4,6-Triisopropylbenzenesulfonyl azideHCID 371707—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물4-Phenyl-3-(3-phenyl-butyryl)-oxazolidin-2-oneHCID 10357976—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(S)-3-((2S,3R)-2-azido-3-phenyl-butyryl)-4-phenyl-oxazolidin-2-oneHCID 8660339641%

반응 단계

Potassium bis(trimethylsilyl)amide (2.0 mL, 1.8 mmol, 0.91 M in tetrahydrofuran) was added to (S)-4-phenyl-3-((S)-3-phenyl-butyryl)-oxazolidin-2-one (500 mg, 1.6 mmol) in anhydrous tetrahydrofuran (8 mL) at −78° C. and stirred for 1 hour. In a separate flask, a solution of 2,4,6-triisopropylbenzenesulphonyl azide (625 mg, 2.0 mmol) in anhydrous tetrahydrofuran (10 mL) at −78° C. was added via cannula to the anion at −78° C. and stirring continued for 2 hours. Acetic acid (0.45 mL, 7.8 mmol) was added to the reaction at −78° C., the mixture warmed to room temperature and stirred overnight. The mixture was poured into water (30 mL) and extracted with ethyl acetate. The combined extracts were washed with brine and dried over sodium sulfate. The crude product was purified on silica gel with 2:1 dichloromethane/hexane to give (S)-3-((2S,3R)-2-azido-3-phenyl-butyryl)-4-phenyl-oxazolidin-2-one (230 mg, 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427635B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-63ca72f3d4f24e16ba1c51f65551f18a
출처 메모uspto-grants-2008_09