참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2-Acetylfuran | HCID 14505 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 2,4-Dimethoxybenzaldehyde | HCID 69175 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1,5-Di(2-furyl)-3-(2,4-dimethoxyphenyl)-1,5-pentanedione | HCID 15001912 | — |
반응 단계
Following the general methods outlined by Weller and Luellen (see above), to a solution of 16.6 g (0.1 mole) of 2,4-dimethoxybenzaldehyde 1 and 20 ml (0.2 mole) of 2-acetylfuran 2 in 100 ml of methanol was added 5.5 g of potassium hydroxide previously dissolved in a small amount of methanol. The resulting mixture was heated to reflux and then stirred overnight at 55° C. The solution was then poured into water acidified with 1N HCl and extracted with CH2Cl2. The CH2Cl2 extracts were dried (Na2SO4) and the solvents removed at high vacuum. The resulting amber oil solidified on standing overnight affording 36.7 g of crude dione 3.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05245038 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-a5d5033460474ef09b7089853a326df4 |
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| 출처 메모 | uspto-grants-1993_09 |
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