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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 714127생성일: 2026년 10월 25일

Potassium Carbonate → tert-butyl[(2S,3E)-1-{[tert-butyl(diphenyl)silyl]oxy}-4-(2-nitrophenyl)but-3-en-2-yl]carbamate

https://huagongshe.com/reaction/714127

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물18-Crown-6HCID 28557—
반응물PhosphoniumHCID 5460504—
반응물(2-Nitrobenzyl)triphenylphosphonium bromideHCID 10885283—
반응물tert-butyl[(2R)-1-{[tert-butyl(diphenyl)silyl]oxy}-3-oxopropan-2-yl]carbamateHCID 89929680—
용매DichloromethaneHCID 6344—
용매1,2-DimethoxyethaneHCID 8071—
생성물tert-butyl[(2S,3E)-1-{[tert-butyl(diphenyl)silyl]oxy}-4-(2-nitrophenyl)but-3-en-2-yl]carbamateHCID 13173405738.1%

반응 단계

A solution of tert-butyl[(2R)-1-{[tert-butyl(diphenyl)silyl]oxy}-3-oxopropan-2-yl]carbamate (3, 3.12 g, 7.3 mmol) in DME (30 ml) was treated with solid (2-nitrobenzyl)(triphenyl)phosphonium bromide(3.76 g, 7.86 mmol) (or any other suitable phosphonium salt), the mixture stirred at room temperature under N2 atmosphere for 30 min and then the reaction flask was charged with a solid mixture of potassium carbonate (1.78 g, 12.86 mmol) and 18-crown-6 (219 mg, 0.83 mmol). The purple mixture was further stirred at the same temperature for 14 h; diluted with DCM, washed with saturated NaHCO3, dried over MgSO4, filtered and concentrated Purified through a chromatographic cartridge of silicagel (50 g) eluted with 10% to 35% EtOAc in hexane to get 1.52 g (38% yield) of title compound as light yellow oil. MS: m/z=569.2 (MNa+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09187415B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-13cfa7bc3a9f4e0a87920188b63cd6d6
출처 메모uspto-grants-2015_11