참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 3(2H)-Furanone, 2,2,5-trimethyl- | HCID 137080 | — |
| 반응물 | 3,4-Difluorobenzaldehyde | HCID 588088 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 5-[2-(3,4-Difluorophenyl)ethenyl]-2,2-dimethyl-3(2H)-furanone | HCID 54177108 | 50% |
반응 단계
To a solution of 3,4-difluorobenzaldehyde (1.9 g, 13.2 mM) and 2,2,5-trimethyl-3(2H)-furanone (2.0 g, 15.9 mM) in ethanol (100 mL), was added 1N aqueous sodium hydroxide (1.6 mL, 1.6 mM). The reaction solution was heated at 50° C. for four hours. After the reaction solution was cooled to room temperature, saturated aqueous sodium chloride (400 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 yellow solid. The crude product was triturated with 10% diethyl ether/pet. ether (50 mL) to give a pale yellow solid (1.66 g, 50% yield), m.p. 105°-106° 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-1f12c2f9cdff4db7a48a19cf27fa8c64 |
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| 출처 메모 | uspto-grants-1991_03 |
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