돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2209277생성일: 2026년 10월 26일

Sodium hydride → 1-(4-Bromo-2-nitro-phenoxy)-cyclopropanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/2209277

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ethyl 1-hydroxycyclopropane-1-carboxylateHCID 2733706—
반응물4-Bromo-1-fluoro-2-nitrobenzeneHCID 2736328—
촉매15-Crown-5HCID 36336—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(4-Bromo-2-nitro-phenoxy)-cyclopropanecarboxylic acid ethyl esterHCID 5834078466.6%

반응 단계

Sodium hydride (60%, 166 mg, 4.15 mmol) was added to a solution of ethyl 1-hydroxycyclopropanecarboxylate (0.41 mL, 3.59 mmol) in THF (10 mL) at room temperature. After 15 min, 3 drops of 15-crown-5 were added followed by 4-bromo-1-fluoro-2-nitrobenzene (0.42 mL, 3.41 mmol). Mixture was stirred at room temperature for 24 hours. After diluting with 50 mL of ethyl acetate, mixture was quenched by addition of brine (25 mL) and layers were separated. Aqueous phase was extracted with ethyl acetate and combined organics were dried (MgSO4), filtered, and concentrated under reduced pressure. Resulting residue was purified via silica gel column chromatography (0-30% ethyl acetate/hexanes) to yield ethyl 1-(4-bromo-2-nitrophenoxy)cyclopropanecarboxylate 7.20 (750 mg)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09376441B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-faca75f7960544ebb89e4f0a3c66e48f
출처 메모uspto-grants-2016_06