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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459300생성일: 2026년 10월 25일

1,2-Dibromoethane → (2S)-3-[4-(2-bromo-ethoxy)-phenyl]2-methoxy-propionic acid ethyl ester

https://huagongshe.com/reaction/459300

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DibromoethaneHCID 7839—
반응물Potassium CarbonateHCID 11430—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물HCID 11390460HCID 11390460—
용매EthanolHCID 702—
생성물(2S)-3-[4-(2-bromo-ethoxy)-phenyl]2-methoxy-propionic acid ethyl esterHCID 58822865—

반응 단계

A mixture containing (2S)-3-(4-hydroxy-phenyl)-2-methoxy-propionic acid ethyl ester obtained in Step 1 (0.223 mol, 50 mg), potassium carbonate (0.446 mol, 50 mg), magnesium sulfate (powdered, 50 mg, 1 g/g), ethylene dibromide (3.35 mol. 628 mg) and EtOH (25 mL) was heated at reflux (78–76° C.) for 24 hours and cool to room temperature. The mixture was heated again to reflux (76.5–77° C.) and 2 mL of ethylene dibromide was added. The mixture was heated for another 12 hours at 79.5–80.1° C. and then cooled to room temperature and vacuum filtered. The filtrate was concentrated under vacuum, and the residue was purified by column chromatography (silica gel, hexanes/ethyl acetate 6:1, Rf 027) to produce a colorless oil. MS (ES) for C14H19BrO4 [M+Na]+: 353.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192982B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-9bdce17b3f9745cbabd0c9c4b53ffb28
출처 메모uspto-grants-2007_03