Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → Methyl 3-bromo-2-fluorobenzoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Trimethyl orthoformate | HCID 9005 | — |
| 반응물 | 3-Bromo-2-fluorobenzoic acid | HCID 2736313 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Methyl 3-bromo-2-fluorobenzoate | HCID 21584505 | 84% |
반응 단계
A solution of 3-bromo-2-fluorobenzoic acid (0.219 g, 1 mmol) in dry methanol (5 mL) under nitrogen was treated with trimethylorthoformate (0.22 mL, 2 mmol) and p-toluenesulfonic acid (catalytic amount), and then heated under reflux. After 16 h, the mixture was evaporated and the residue partitioned between water and Et2O. the organic layer was washed with sat. sodium hydrogen carbonate solution, water, brine, dried (MgSO4) and evaporated to give methyl 3-bromo-2-fluorobenzoate (0.195 g, 0.84 mmol, 84%): 1H-NMR (CDCl3) δ7.90-7.85 (m, 1H), 7.71-7.65 (m, 1H), 7.10 (dt, 1H, J=8.0, 1.0 Hz), 3.94 (s, 3H): MS (EI) 232 (M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06566358B2 |
| 출처 데이터셋 | uspto-grants-2003_05 |
| ORD ID | ord-41d7a8e3aab14b49a84d863e7faaf206 |
| 출처 메모 | uspto-grants-2003_05 |