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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 970637생성일: 2026년 10월 26일

Chlorotrimethylsilane → (S)-tert-butyl 4-((R)-4-ethoxy-4-oxobutan-2-yl)-2,2-dimethyloxazolidine-3-carboxylate

https://huagongshe.com/reaction/970637

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Lithium BromideHCID 82050—
반응물(S,E)-tert-butyl 4-(3-ethoxy-3-oxoprop-1-enyl)-2,2-dimethyloxazolidine-3-carboxylateHCID 10732902—
반응물Ammonium chloride ammonium hydroxideHCID 21863491—
반응물HCID 178418348HCID 178418348—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TetrahydrofuranHCID 8028—
생성물(S)-tert-butyl 4-((R)-4-ethoxy-4-oxobutan-2-yl)-2,2-dimethyloxazolidine-3-carboxylateHCID 11336032—

반응 단계

To CuI (3.36 g, 17.64 mmol) in THF (15 mL) was added at −78° C. MeLi.LiBr (1.5M in ether, 23.5 mL, 35.28 mmol), and the resulting mixture was stirred at −78° C. for 15 min. TMSCl (1.52 mL, 17.64 mmol) and Me2CuLi (generated above) were added in sequence at −78° C. to (S,E)-tert-butyl 4-(3-ethoxy-3-oxoprop-1-enyl)-2,2-dimethyloxazolidine-3-carboxylate (0.88 g, 2.94 mmol), and the resulting mixture was slowly warmed up to rt. Ammonium chloride-ammonium hydroxide buffer (pH ˜8) was added to the reaction mixture. The mixture was extracted with ether, washed with brine, dried over sodium sulfate, and concentrated. Flash chromatography (silica gel, 2:8=ethyl acetate:hexanes) gave (S)-tert-butyl 4-((R)-4-ethoxy-4-oxobutan-2-yl)-2,2-dimethyloxazolidine-3-carboxylate as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07312218B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-7d8d6197b34c466986f01dabcd3cfa73
출처 메모uspto-grants-2007_12