참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 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 | 62.6% |
반응 단계
A reactor vessel is charged with 3-amino-2-chloropyridine (2.7 g, 21 mmol), 2,2,2-trifluoroethanol (15 g, 150 mmol), and trifluoroacetic acid (3.63 g, 31.8 mmol). The solution is cooled to the range 0° C. to 5° C. and then the reagent t-butyl nitrite (2.51 g of a 96% solution, 23.4 mmol) is added drop-wise to the vessel maintaining the temperature in the range 0° C. to 5° C. After stirring a few minutes the solution is transferred drop-wise to a reactor vessel containing 2,2,2-trifluoroethanol (20 g, 200 mmol) maintained at 55° C. The temperature rose to 70° C. during the drop-wise addition of the diazonium salt reaction mass. After cooling the solution, it 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 (3.36 g) with an actual yield of 62.6%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06710180B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-6692566b87734cbdb07afed6ba1ac6e2 |
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| 출처 메모 | uspto-grants-2004_03 |
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