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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133842생성일: 2026년 10월 26일

2,4,6-Triisopropylbenzenesulfonyl azide → (4S)-3-[(2S)-2-azido-3-methyl-3-phenylbutanoyl]-4-benzyl-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/133842

반응식

참여 물질

역할이름HCID투입량
반응물2,4,6-Triisopropylbenzenesulfonyl azideHCID 371707—
반응물PotassiumHCID 5462222—
반응물(4S)-4-benzyl-3-(3-methyl-3-phenylbutanoyl)-1,3-oxazolidin-2-oneHCID 10472250—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물(4S)-3-[(2S)-2-azido-3-methyl-3-phenylbutanoyl]-4-benzyl-1,3-oxazolidin-2-oneHCID 1040730396.9%

반응 단계

A solution of (4S)-4-benzyl-3-(3-methyl-3-phenylbutanoyl)-1,3-oxazolidin-2-one (1.0 g, 3.0 mmol, from Reference Example 26) in anhydrous tetrahydrofuran (16 mL) is cooled to −78° C. in a dry-ice/acetone bath while stirring under a nitrogen atmosphere. Potassium hexamethylsilazide (0.5 M solution in toluene, 6.6 mL, 3.3 mmol) is added dropwise to the solution via syringe. After stirring for 1 hour at −78° C., trisyl azide (1.2 g, 3.8 mmol) in tetrahydrofuran (8 mL) is added dropwise. The reaction mixture is stirred for 2-3 minutes at −78° C. and then quenched by the addition of glacial acetic acid (0.8 mL). Stirring is continued for 1 hour at 40° C. The reaction mixture is diluted with brine and diethyl ether. The aqueous phase is extracted thrice with diethyl ether. The combined extracts are washed with saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride, dried over sodium sulfate, decanted, and concentrated under reduced pressure to afford a white/yellow solid. The crude material is purified by flash chromatography (ethyl acetate/hexanes) to afford a clear, straw colored oil (1.1 g, 79%). TOF MS (ES+): (M+H)=379.2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390910B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-a2d6f9d651e540708234ef0796a29fa6
출처 메모uspto-grants-2008_06