Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Formic Acid → N-(2-fluoro-4-iodophenyl)formamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Formic Acid | HCID 284 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | 2-Fluoro-4-iodoaniline | HCID 185694 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-(2-fluoro-4-iodophenyl)formamide | HCID 23549341 | 97.1% |
반응 단계
To a cooled solution (0° C.) of 4-iodo-2 fluoroaniline (3.05 g, 12.9 mmol) in tetrahydrofuran (15 mL) and toluene (15 mL), was slowly added a mixture of acetic anhydride (1.39 mL, 14.7 mmol) and formic acid (0.83 mL, 22.0 mmol). The reaction mixture was stirred at rt overnight, then diluted with ethyl acetate (100 mL) and 1N aqueous HCl (100 mL). The layers were separated, and the organic layer was washed with water and saturated sodium carbonate solution, and dried over sodium sulfate. The solvent was removed under reduced pressure to afford 2-fluoro-4-iodophenylformamide as an off-white solid (3.32 g, 97%). GC-MS ret. time 2.27 min, m/z 265 (M+); 1H NMR (300 MHz, CDCl3) δ: 7.37-7.51 (m, 3H), 8.13 (t, 1H), 8.46 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07423156B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-22b4e1dc687b469fadcc66f83c4a3b41 |
| 출처 메모 | uspto-grants-2008_09 |