Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2,5-Dichlorophenol → 4-(2,5-Dichlorophenoxy)-3-nitrobenzonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2,5-Dichlorophenol | HCID 66 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Benzonitrile, 4-chloro-3-nitro- | HCID 13655 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-(2,5-Dichlorophenoxy)-3-nitrobenzonitrile | HCID 59548942 | 81.8% |
반응 단계
2,5-Dichlorophenol (17.86 g, 109.54 mmol) and 4-chloro-3-nitrobenzonitrile (10.00 g, 54.77 mmol) were combined with K2CO3 (37.85 g, 273.85 mmol) in THF (300 mL). The reaction mixture was refluxed for 48 hrs and then the solid was filtered over a bed of Celite. After rinsing the residue with copious amounts of DCM, the filtrate was concentrated to produce a yellow solid. The solid was triturated with minimal DCM and collected via vacuum filtration to yield compound 34 (13.84 g, 81.7% yield, 100.0% pure). 1H NMR (500 MHz, DMSO-d6): δ 8.73 (s, 1H), 8.12 (dd, J1=9 Hz, J2=2 Hz, 1H), 7.73 (d, J=9 Hz, 1H), 7.65 (d, J=2 Hz, 1H), 7.48 (dd, J1=9 Hz, J2=2 Hz, 1H), 7.21 (d, J=9 Hz, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08399456B2 |
| 출처 데이터셋 | uspto-grants-2013_03 |
| ORD ID | ord-c6845f4a525f42d7a7b4b65c46ef0020 |
| 출처 메모 | uspto-grants-2013_03 |