Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanesulfonic Acid → 2-Chloro-3-(2,2,2-trifluoroethoxy)pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 반응물 | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| 반응물 | Tert-Butyl nitrite | HCID 10906 | — |
| 반응물 | 2-Chloro-3-pyridylamine | HCID 80528 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | 2-Chloro-3-(2,2,2-trifluoroethoxy)pyridine | HCID 12056728 | 67.3% |
반응 단계
A reactor vessel is charged with 3-amino-2-chloropyridine (5.4 g, 42 mmol), 2,2,2-trifluoroethanol (50 g, 500 mmol), and methanesulfonic acid (4.1 g, 43 mmol). The solution is heated to the range 55° C. to 60° C. and then t-butyl nitrite (5.3 g of a 90% solution, 46 mmol) is added drop-wise to the vessel while maintaining the temperature at 60° C. to 65° C. After nitrogen evolution ceases, the solution is cooled, neutralized with aqueous saturated sodium bicarbonate solution and then extracted with MTBE. The solvent is removed by evaporation to obtain 2-chloro-3-(2,2,2-trifluoroethoxy)pyridine as a crude oil (11.1 g) with an actual yield of 67.3%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06710180B2 |
| 출처 데이터셋 | uspto-grants-2004_03 |
| ORD ID | ord-178acea5fc59416fa07e80f9c264941c |
| 출처 메모 | uspto-grants-2004_03 |