참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| 반응물 | Undec-4-ene | HCID 136496 | — |
| 반응물 | 2,5-dimethyl-2-phenyl-3(2H)-furanone | HCID 15086699 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-Methyl-2-phenyl-5-[2-(2-pyridinyl)ethenyl]-3(2H)-furanone | HCID 54430754 | 40% |
반응 단계
To a solution of 2-pyridinecarboxaldehyde (1.2 mL, 1.2 mM) and 2,5-dimethyl-2-phenyl-3(2H)-furanone (1.5 g, 8 mM) in ethanol (15 mL), was added 1,8-diazebicyclo[4.5.0]undec-7ene (DBU, 0.2 mL, 1.3 mM). The reaction solution was heated at 80° C. for 5 hours. After the reaction solution cooled to room temperature, saturated aqueous sodium chloride (400 mL) was added. The aqueous layer was extracted with dichloromethane (3×100 mL). The combined dichloromethane extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give a yellow solid. Purification by trituration with 10% diethyl ether in hexane gave a pale pink solid (887 mg, 40% yield), m.p. 74.5°-76° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05001126 |
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| 출처 데이터셋 | uspto-grants-1991_03 |
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| ORD ID | ord-06b83c91a9b2484ea66f8a07b806b0af |
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| 출처 메모 | uspto-grants-1991_03 |
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