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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,4,6-Triisopropylbenzenesulfonyl azide | HCID 371707 | — |
| 반응물 | Potassium | HCID 5462222 | — |
| 반응물 | (4S)-4-benzyl-3-(3-methyl-3-phenylbutanoyl)-1,3-oxazolidin-2-one | HCID 10472250 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (4S)-3-[(2S)-2-azido-3-methyl-3-phenylbutanoyl]-4-benzyl-1,3-oxazolidin-2-one | HCID 10407303 | 96.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07390910B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-a2d6f9d651e540708234ef0796a29fa6 |
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| 출처 메모 | uspto-grants-2008_06 |
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