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HRID 32837作成日:2026年10月26日

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

https://huagongshe.com/reaction/32837

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物2,4,6-Triisopropylbenzenesulfonyl azideHCID 371707—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物4-Phenyl-3-(3-phenyl-butyryl)-oxazolidin-2-oneHCID 10357976—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-3-((2S,3R)-2-azido-3-phenyl-butyryl)-4-phenyl-oxazolidin-2-oneHCID 8660339641%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427635B2
出典データセットuspto-grants-2008_09
ORD IDord-63ca72f3d4f24e16ba1c51f65551f18a
出典メモuspto-grants-2008_09