Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
5-Chloro-2-nitrobenzoic acid → 3-Amino-5-chloro-2-nitrobenzoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 5-Chloro-2-nitrobenzoic acid | HCID 17286 | — |
| 반응물 | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 촉매 | Cupric acetate | HCID 8895 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-Amino-5-chloro-2-nitrobenzoic acid | HCID 10727479 | 100.5% |
반응 단계
Under nitrogen, to a solution of t-BuOK (156.8 g) and Cu(OAc)2 (3.6 g) in DMF (1.2 L) was added a solution of 5-chloro-2-nitrobenzoic acid (40.0 g) and MeONH2HCl (33.2 g) in DMF (300 mL) at 0° C. After 3 h the reaction was quenched by addition of H2O (2.5 L) and acidified with 10% HCl solution to pH=1. The mixture was extracted with EA (2 L×2) and the combined organic layers were then washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in-vacuo to afford the crude product as a yellow solid (43.2 g, yield 100%). 1H NMR (300 MHz, CDCl3): δ ppm 6.88 (s, 1H, J=2.4 Hz), 6.91 (d, 1H, J=2.4 Hz), 8.08 (br s, 2H); LC-MS: m/e=217 [M+1]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08541411B2 |
| 출처 데이터셋 | uspto-grants-2013_09 |
| ORD ID | ord-2e39807bb5a247ceb9d93ca56ec7de94 |
| 출처 메모 | uspto-grants-2013_09 |