関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2-Acetylfuran | HCID 14505 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 2,4-Dimethoxybenzaldehyde | HCID 69175 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1,5-Di(2-furyl)-3-(2,4-dimethoxyphenyl)-1,5-pentanedione | HCID 15001912 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05245038 |
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| 出典データセット | uspto-grants-1993_09 |
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| ORD ID | ord-a5d5033460474ef09b7089853a326df4 |
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| 出典メモ | uspto-grants-1993_09 |
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