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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38110생성일: 2026년 10월 23일

Water → 1-(benzyloxy)-4-((1R,2S)-2-nitrocyclopropyl)benzene

https://huagongshe.com/ko/reaction/38110

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
반응물(E)-1-(Benzyloxy)-4-(2-nitrovinyl)benzeneHCID 5702926—
반응물Potassium tert-butoxideHCID 23665647—
용매Dimethyl SulfoxideHCID 679—
생성물1-(benzyloxy)-4-((1R,2S)-2-nitrocyclopropyl)benzeneHCID 6662958326%

반응 단계

Trimethylsulfoxonium iodide (0.62 g, 2.82 mmol) was added in portions to a solution of t-BuOK (0.32 g, 2.82 mmol) in dry DMSO (5 mL). After 10 min a solution of 1-(benzyloxy)-4-[(E)-2-nitrovinyl]benzene (0.60 g, 2.35 mmol) in DMSO (5 mL) was transferred via canula and the mixture was stirred at room temperature for 6 h. The reaction was poured over water (10 mL) and extracted with Et2O (3×10 mL); the organic layers were washed with brine (2×15 mL), dried over anhydrous Na2SO4 and filtered. After removal of the solvent, the residual orange oil was purified by column chromatography on silica gel (5% EtOAc/hexanes) affording 0.16 g of 1-(benzyloxy)-4-[(1R,2S)-2-nitrocyclopropyl]benzene [Rf=0.5 (20% EtOAc/hexanes), white solid, 26% yield].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524717B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-fe87a081692640108b1b12d04c59faba
출처 메모uspto-grants-2013_09