Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzoyl Peroxide → (E)-4-bromo-3-(2-propyl-phenoxy)-but-2-enoic acid ethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzoyl Peroxide | HCID 7187 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | (E)-3-(2-propyl-phenoxy)-but-2-enoic acid ethyl ester | HCID 66895388 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 생성물 | (E)-4-bromo-3-(2-propyl-phenoxy)-but-2-enoic acid ethyl ester | HCID 66894945 | 49.7% |
반응 단계
To a stirred mixture of (E)-3-(2-propyl-phenoxy)-but-2-enoic acid ethyl ester (3.10 g, 0.012 mol) in carbon tetrachloride (20 mL) under a nitrogen atmosphere was added N-bromosuccinimide (3.30 g, 0.019 mol) and benzoyl peroxide (300 mg, 0.001 mol). Nitrogen gas was bubbled through the mixture for 5 min, and the resulting mixture was heated to reflux for 4 h. The reaction mixture was then placed in the refrigerator overnight. The solids formed were removed by filtration and the filtrate concentrated in vacuo. The crude product obtained was purified using flash column chromatography (silica gel (100-200 mesh), ethyl acetate/hexanes) to afford (E)-4-bromo-3-(2-propyl-phenoxy)-but-2-enoic acid ethyl ester (1.95 g, 48%) as a yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07741327B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-f6b1e0cceea243638295320e584a8d61 |
| 출처 메모 | uspto-grants-2010_06 |