참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 7,8-Dihydroxyflavone | HCID 1880 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | 1-Butyne, 3-chloro-3-methyl- | HCID 70679 | — |
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 생성물 | 7,8-Bis-(1,1-dimethyl-prop-2-ynyloxy)-2-phenyl-chromen-4-one | HCID 59052279 | 69% |
반응 단계
To a suspension of 7,8-dihydroxy-2-phenyl-chromen-4-one (510 mg, 2 mmol) and CuCl2 (16 mg, 0.12 mmol) in acetonitrile (3 mL) was added 3-chloro-3-methyl-1-butyne (0.5 mL, 4.56 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.78 mL, 5.2 mmol) slowly at 0° C. The dark mixture was stirred at 0° C. for 5 h and then at room temperature overnight. The solvent was evaporated and the residue was purified by column chromatography (SiO2, EtOAc:hexanes/10-50%) to give the title compound as a white solid (540 mg, 69%): 1H NMR (CDCl3, 300 MHz) δ 8.02 (m, 2H), 7.96 (d, J=9.0 Hz, 1H), 7.69 (d, J=9.0 Hz, 1H), 7.53 (m, 3H), 6.78 (s, 1H), 2.66 (s, 1H), 2.26 (s, 1H), 1.81 (s, 6H), 1.76 (s, 6H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07592143B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-9bcbb5461b234b19b6e606b26e50ecfb |
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| 출처 메모 | uspto-grants-2009_09 |
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