Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Allyl bromide → 2-(Allyloxy)-1-bromo-5-methyl-3-nitrobenzene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Allyl bromide | HCID 7841 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Bromo-4-methyl-6-nitrophenol | HCID 29918 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2-(Allyloxy)-1-bromo-5-methyl-3-nitrobenzene | HCID 14977444 | 94.2% |
반응 단계
To a mixture of 2-bromo-4-methyl-6-nitrophenol (7.00 g, 30.2 mmol), K2CO3 (6.26 g, 45.3 mmol) in acetone (105 mL) was added allyl bromide (3.80 ml, 45.3 mmol). The reaction mixture was stirred at room temperature overnight. It was then heated at 40° C. for 5 hrs. Inorganic salts were filtered and washed with acetone. The filtrate was concentrated to give 7.74 g (94%) of the desired product. MS (DCI/NH3) m/z: 289.0 (M+NH4)+; 1H NMR (300 MHz, CD3OD) δ ppm 2.37 (s, 3 H) 4.61 (d, J=6.10 Hz, 2 H) 5.26 (dd, J=10.51, 1.80 Hz, 1 H) 5.39 (dd, J=17.29, 1.80 Hz, 1 H) 6.09 (m, 1 H) 7.63 (s, 1 H) 7.74 (s, 1 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07163939B2 |
| 출처 데이터셋 | uspto-grants-2007_01 |
| ORD ID | ord-45249ef8d80d45258c2767c58c8dce87 |
| 출처 메모 | uspto-grants-2007_01 |