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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523175생성일: 2026년 10월 25일

Sodium Acetate → (2R,3S)-tert-butyl 2-ethyl-3-formylaziridine-1-carboxylate

https://huagongshe.com/reaction/523175

반응식

참여 물질

역할이름HCID투입량
반응물Sodium AcetateHCID 517045—
반응물N-Boc-p-toluenesulfonamideHCID 688170—
반응물(E)-2-PentenalHCID 5364752—
반응물(S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl EtherHCID 11198150—
용매ChloroformHCID 6212—
생성물(2R,3S)-tert-butyl 2-ethyl-3-formylaziridine-1-carboxylateHCID 90121328—

반응 단계

To a 500 mL round-bottom flask equipped with a stir bar was added (S)-2-(diphenyl((trimethylsilyl)oxy)methyl)pyrrolidine (2.60 g, 8.00 mmol) and CHCl3 (200 mL). To the solution was added tert-butyl tosylcarbamate (10.9 g, 40.0 mmol). The flask was placed in a room temperature-water bath. To the stirred solution was added sodium acetate (9.84 g, 120 mmol), then (E)-pent-2-enal (4.04 g, 48.0 mmol). The mixture was stirred at room temperature for 40 minutes. The mixture was filtered, washing the filter cake with a small amount of CHCl3. The filtrate was concentrated in vacuo at 30° C. The resulting orange liquid was dissolved in Et2O (400 mL) and transfered to a 1 L separatory funnel. The solution was washed with water:aq. sat. NaHCO3 (200 mL:200 mL). The aqueous phase was extracted with Et2O (100 mL). The combined organics were washed with brine (200 mL); dried over MgSO4; filtered; then concentrated in vacuo to afford (2R,3S)-tert-butyl 2-ethyl-3-formylaziridine-1-carboxylate as a pale orange liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334279B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-74e9e9d7f9554b9fa6d24097e1c753d9
출처 메모uspto-grants-2016_05