참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 2,5-dimethyl-2-phenyl-3(2H)-furanone | HCID 15086699 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-Phenyl-2-methyl-5-[2-(3-pyridinyl)ethenyl]-3(2H)-furanone | HCID 54185767 | 54.3% |
반응 단계
To a solution of 3-pyridinecarboxaldehyde (1.03 g, 9.6 mM) and 2,5-dimethyl-2-phenyl-3(2H)-furanone (1.0 g, 8 mM) in ethanol (50 mL), was added 1N aqueous sodium hydroxide (2.4 mL, 2.4 mM). The reaction solution was heated at 60° C. for 8 hours. After the reaction solution cooled to room temperature, saturated aqueous sodium chloride (200 mL) was added. The aqueous layer was extracted with diethyl ether (3×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give a brown solid. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to afford a yellow crystalline solid (0.8 g, 36.3% yield), m.p. 106°-108° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05010102 |
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| 출처 데이터셋 | uspto-grants-1991_04 |
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| ORD ID | ord-85ab62e24ea14702b94e6f7291dee02b |
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| 출처 메모 | uspto-grants-1991_04 |
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