Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 3-(4-Nitro-thiophen-2-ylmethylene)-3H-isobenzofuran-1-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Nitrothiophene-2-carbaldehyde | HCID 818857 | — |
| 반응물 | HCID 86628633 | HCID 86628633 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 3-(4-Nitro-thiophen-2-ylmethylene)-3H-isobenzofuran-1-one | HCID 68910119 | — |
반응 단계
To a solution of (4-oxo-3,4-dihydro-phthalazin-1-yl)-phosphonic acid dimethyl ester (3.85 g, 15.9 mmol) in THF (30 mL) was added 4-nitro-thiophene-2-carbaldehyde (25) (2.5 g, 15.9 mmol) under nitrogen. Triethylamine (2.2 mL 15.9 mmol) was added dropwise over 10 minutes and then stirred at room temperature for 4 hours. The yellow suspension was poured in water (80 mL), and the then filtered, the solid was washed with water (15 mL), hexane (10 mL) and then diethyl ether (10 mL) and then dried in vacuo to afford a 4.1 g of the desired products. Two peaks in LC-MS analysis, (4.1 g, 94%) and required no further purification; m/z (LC-MS, ESP), RT=4.71 mins (M+H) 274, & RT=4.84 mins (M+H) 274;
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07902193B2 |
| 출처 데이터셋 | uspto-grants-2011_03 |
| ORD ID | ord-4d90028aa22a4d56ac086b9fbf7ce389 |
| 출처 메모 | uspto-grants-2011_03 |