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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1039729생성일: 2026년 10월 25일

Imidazole → Tributylphosphine oxide

https://huagongshe.com/reaction/1039729

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물TributylphosphineHCID 13831—
반응물Sodium hydrideHCID 24758—
반응물(S)-tert-butyl 2-((S)-1,2-bis(tert-butyldimethylsilyloxy)ethyl)aziridine-1-carboxylateHCID 86635713—
용매TolueneHCID 1140—
생성물Tributylphosphine oxideHCID 13138—
생성물tert-butyl (2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-(1H-imidazol-1-yl)butan-2-ylcarbamateHCID 57950888—

반응 단계

A solution of (5)-tert-butyl 2-((S)-1,2-bis(tert-butyldimethylsilyloxy)ethyl)aziridine-1-carboxylate (0.740 g, 1.7 mmol) and 1H-imidazole (0.35 g, 5.1 mmol) in 3 mL toluen was thoroughly degassed and treated with tributylphosphine (0.42 ml, 1.7 mmol). The reaction mixture was heated to reflux and allowed to stir for 3 hours. NaH (60% dispersion in mineral oil) (0.069 g, 2.9 mmol) was added and the reaction mixture was allowed to stir at 110° C. overnight. The reaction mixture was quenched with saturated NH4Cl solution and diluted with EtOAc. The reaction mixture was washed with water then brine. The organics were dried over MgSO4 and concentrated in vacuo. Purification of the crude residue by column chromatography gave tert-butyl (2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-(1H-imidazol-1-yl)butan-2-ylcarbamate with tributylphosphine oxide as the major impurity. This material was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08552181B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-fca6ca29bd5b4a0cb7261eb70aaef559
출처 메모uspto-grants-2013_10