Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
(+-)-3-Methyl-2,4(3H,5H)-furandione → 6-fluoro-3-(4-methoxy-5H-furan-2-ylidene)-1,3-dihydro-indol-2-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | (+-)-3-Methyl-2,4(3H,5H)-furandione | HCID 544553 | — |
| 반응물 | 6-fluoro-2,3-dihydro-1H-indol-2-one | HCID 3731013 | — |
| 반응물 | LiHMDS tetrahydrofuran | HCID 23714775 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-fluoro-3-(4-methoxy-5H-furan-2-ylidene)-1,3-dihydro-indol-2-one | HCID 69401606 | — |
반응 단계
To a stirred solution of 6-fluorooxindole (2.6 g, 17.5 mmol) in anhydrous THF (30 mL) under nitrogen was added 1.0 M LiHMDS/THF solution (35 mL, 35 mmol). The mixture was stirred at room temperature for 10 minutes. Methyl tetronate (1.0 g, 8.8 mmol) was added as one portion. After stirring at room temperature for 1 hour, the reaction was cooled to 0° C., and quenched with 2M HCl until pH=3. The mixture was stirred at room temperature for 2 more hours, and poured into 250 mL of water. The resulting precipitates were filtered, rinsed with water and dried in vacuum to give 6-fluoro-3-(4-methoxy-5H-furan-2-ylidene)-1,3-dihydro-indol-2-one as off-white solid. Yield: 840 mg, 38%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08367664B2 |
| 출처 데이터셋 | uspto-grants-2013_02 |
| ORD ID | ord-b1efd9c2b7b045e18a00bbc540fa478f |
| 출처 메모 | uspto-grants-2013_02 |