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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21978생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/21978

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 warned 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 번호US05426103
출처 데이터셋uspto-grants-1995_06
ORD IDord-abd37e9569de41e18c1a8ba201ccfeea
출처 메모uspto-grants-1995_06