참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 1-Iodo-4-nitrobenzene | HCID 12495 | — |
| 반응물 | Bromodifluoromethyl diethylphosphonate | HCID 144101 | — |
| 촉매 | Cuprous chloride | HCID 62652 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Diethyl[(4-nitrophenyl)(difluoro)methyl]phosphonate | HCID 10881410 | 86.4% |
반응 단계
Under N2, a mixture of bromodifluoromethyl diethylphosphonate (0.427 g, 1.6 mmol) and Cd powder (180 mg, 1.6 mmol) in DMF (0.5 mL) was stirred at room temperature for 2 h. Most of Cd disappeared. 4-Iodo-1-nitrobenzene (249 mg, 1.00 mmol) and CuCl (115 mg, 1.16 mmol) were then added. The mixture was again stirred at room temperature for 3 h. Ether (20 mL) was added to the reaction mixture and the precipitated solids were filtered off and washed with 10 mL of ether. The combined ether layers were washed with NH4Cl (aq), dried over MgSO4, and evaporated to give the title product (267 mg, yield: 86%). 1H NMR (CD3OD, 400 MHz): δ=1.33 (t, J=7.2 Hz, 6 H), 4.20-4.28 (m, 4 H), 7.86 (d, J=8.4 Hz, 2 H), 8.39 (d, J=8.4 Hz, 2 H). MS (ES+): m/z 310.06 [MH+]. HPLC: tR=3.92 min (ZQ3, polar—5 min).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09096624B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-74edbd9c43fd48d09099dde919adc8eb |
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| 출처 메모 | uspto-grants-2015_08 |
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