Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-Iodosuccinimide → 3-Bromo-2-iodo-5-(trifluoromethyl)aniline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-Iodosuccinimide | HCID 120273 | — |
| 반응물 | 3-Bromo-5-(trifluoromethyl)aniline | HCID 2735880 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 3-Bromo-2-iodo-5-(trifluoromethyl)aniline | HCID 57546142 | — |
반응 단계
3-Bromo-5-(trifluoromethyl)aniline (20 g, 83 mmol) in acetic acid (150 ml) was treated portionwise with N-iodosuccinimide (20.62 g, 92 mmol). The reaction was stirred 24 h at ambient temperature. The reaction was diluted with ethyl acetate (600 mL) and was washed with aqueous sodium bisulfie (100 mL) and brine (100 mL). The organic layer was dried with magnesium sulfate and evaporated. The residue was purified on a silica gel column with a gradient of ethyl acetate/hexanes from 7% to 15% to give 23.5 g (77%) of slightly impure product. 1H-NMR (CDCl3, 400 MHz) δ 7.21 (d, J=1.3 Hz, 1H), 6.82 (d, J=1.5 Hz, 1H), 4.57 (bs, 2H); LC/MS (HPLC method 4): tR=3.578 min, 365.80(MH)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08026257B2 |
| 출처 데이터셋 | uspto-grants-2011_09 |
| ORD ID | ord-24bf3eb8f2554ac5ae473672e1b1b61d |
| 출처 메모 | uspto-grants-2011_09 |