참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | m-Ethynylphenol | HCID 139144 | — |
| 반응물 | 1-(Difluoromethoxy)-4-iodobenzene | HCID 2737008 | — |
| 촉매 | Copper iodide | HCID 83717 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-((4-(Difluoromethoxy)phenyl)ethynyl)phenol | HCID 59790321 | — |
반응 단계
A solution of 4-(difluoromethoxy)phenyl iodide (4.70 g) in deoxygenated dimethylformamide was treated with trans-dichlorobis(triphenylphosphine) palladium(II) (244 mg) and copper(II) iodide 66 mg) followed by triethylamine (7.52 mL), stirred under a nitrogen atmosphere for 5min., treated with 3-hydroxyphenyl acetylene (2.467 g), stirred under nitrogen atmosphere for 16 h, poured into ethyl acetate and was washed with 0.05 N HCl and water. The organic phase was dried over MgSO4 and concentrated in vacuo. The residue was chromatographed, silica gel, 40% ethyl acetate/hexane as eluent, to afford 3-((4-(difluoromethoxy)phenyl)ethynyl)phenol as a tan solid, 5.40 g; 1H NMR (DMSO-d6): δ 9.64 (s, 1H), 7.56 (d, J=8.8 Hz, 2H), 7.27 (t, J=73.7 Hz, 1H), 7.17 (d, J=8.8 Hz, 2H), 7.16 (m, 1H), 6.94 (m, 1H), 6.86 (m, 1H), and 6.77 (m, 1H); MS (ES neg) m/z 260.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423158B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-d89ce363547847d1ae42f1a34706a5ac |
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| 출처 메모 | uspto-grants-2008_09 |
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