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Methanesulfonic Acid → 2-Chloro-3-(2,2,2-trifluoroethoxy)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 反応物 | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| 反応物 | Tert-Butyl nitrite | HCID 10906 | — |
| 反応物 | 2-Chloro-3-pyridylamine | HCID 80528 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 生成物 | 2-Chloro-3-(2,2,2-trifluoroethoxy)pyridine | HCID 12056728 | 67.3% |
反応手順
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%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06710180B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-178acea5fc59416fa07e80f9c264941c |
| 出典メモ | uspto-grants-2004_03 |