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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5405생성일: 2026년 10월 24일

tert-Butyl Dimethylphosphonoacetate → Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate

https://huagongshe.com/ko/reaction/5405

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl DimethylphosphonoacetateHCID 4564495—
반응물Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylateHCID 19930804—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylateHCID 54383214—

반응 단계

Potassium hexamethyldisilylamide (40.5 mL of a 0.58M solution in toluene, 23.5 mmol) is added to THF (60 mL), and then cooled to 0° C. t-Butyl dimethylphosphonoacetate (4.6 mL, 23.5 mmol) is added dropwise, and the reaction is warmed to room temperature and stirred for 25 minutes. Ethyl 2,3-di-oxo-1-azacyclodecane-10-carboxylate (2.83 g, 11.74 mmol) is added in THF (15 mL), and the reaction is stirred at room temperature for 2.5 hours. The reaction is quenched with saturated ammonium chloride, and then extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244889
출처 데이터셋uspto-grants-1993_09
ORD IDord-9f6126e0435c45d1b9864f1d5abc955e
출처 메모uspto-grants-1993_09