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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,2-Dibromoethane | HCID 7839 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| 반응물 | HCID 11390460 | HCID 11390460 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | (2S)-3-[4-(2-bromo-ethoxy)-phenyl]2-methoxy-propionic acid ethyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07192982B2 |
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| 출처 데이터셋 | uspto-grants-2007_03 |
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| ORD ID | ord-9bdce17b3f9745cbabd0c9c4b53ffb28 |
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| 출처 메모 | uspto-grants-2007_03 |
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