Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,3,3,3-Tetrafluoro-1-methoxy-2-(trifluoromethyl)-1-propene → 4-Fluoro-6-methoxy-5-(trifluoromethyl)pyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,3,3,3-Tetrafluoro-1-methoxy-2-(trifluoromethyl)-1-propene | HCID 9672 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Formamidine acetate | HCID 160693 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Fluoro-6-methoxy-5-(trifluoromethyl)pyrimidine | HCID 58439251 | — |
반응 단계
To a rapidly stirred mixture of 1,1,1,3-tetrafluoro-2-(trifluoromethyl)-4-oxapent-2-ene (N-1) (10.0 g, 47.15 mmol) and formamidine acetate (7.37 g, 70.73 mmol) in a mixture of water (50 mL) and dichloromethane (50 mL) at 0° C., a solution of sodium hydroxide (7.54 g, 189 mmol) in water (40 mL) is added dropwise and the resulting mixture is stirred for 30 min after complete addition. The dichloromethane layer is separated, washed with 1M aqueous HCl solution and water, dried over Na2SO4 and filtered. The filtrate is concentrated in vacuo to afford 4-fluoro-6-methoxy-5-(trifluoromethyl)pyrimidine (N-2) as a yellow solid. The product is used directly in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08604032B2 |
| 출처 데이터셋 | uspto-grants-2013_12 |
| ORD ID | ord-4df9d1f9ff3045cfaa39b8226f2bb6b6 |
| 출처 메모 | uspto-grants-2013_12 |