참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | 2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate | HCID 58926348 | — |
| 촉매 | Benzyl triethylammonium chloride | HCID 66133 | — |
| 촉매 | HCID 178418476 | HCID 178418476 | — |
| 용매 | Toluene water | HCID 22272177 | — |
| 생성물 | 4-(4-methoxyphenyl)-5,5-dimethylfuran-2(5H)-one | HCID 58926254 | — |
반응 단계
To a 1:1 mixture of toluene/water (20 mL), were added 2,2-dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate (100 mg, 0.38 mmol), 4-methoxyphenylboronic acid (87 mg, 0.57 mmol), PdCl2(PPh3)2 (27 mg, 0.038 mmol), 2M KF aqueous solution (0.95 mL, 1.9 mmol), benzyltriethylammonium chloride (8.7 mg, 0.038 mmol). The mixture was heated at 50° C. under N2 for 30 minutes, cooled to room temperature and extracted with EtOAc (2×50 mL). The organic layers were combined, washed with saturated NaHCO3 (50 mL) and brine (50 mL), dried over Na2SO4. Purification through silica gel column with 10-30% EtOAc/hexanes led to the product as yellow solid. Yield: 33 mg, 40%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08877923B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-7bf0b10118034bb1bb14191273d87519 |
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| 출처 메모 | uspto-grants-2014_11 |
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