関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3,4,5-Trimethoxybenzaldehyde | HCID 6858 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 3(2H)-Furanone, 2,2,5-trimethyl- | HCID 137080 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2,2-Dimethyl-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]-3(2H)-furanone | HCID 53716106 | 83% |
反応手順
To a mixture of 2,2,5-trimethyl-3(2H)-furanone (2.5 g, 19.8 mM) and 3,4,5-trimethoxybenzaldehyde (4.7 g, 23.8 mM) in ethanol was added 1N aqueous sodium hydroxide (4 mL, 4mM). After the reaction mixture was stirred for 48 hours at room temperature, the solution was concentrated to 50 mL and diluted with water (300 mL). The aqueous layer was extracted with diethyl ether (4×100 mL). The combined ethereal extracts were washed with saturated aqueous sodium chloride (50 mL), dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford a dark yellow crystalline solid. The crude product was purified by chromatography (silica gel, petroleum ether-ethyl acetate) to give light yellow crystals (5.0 g, 83% yield), m.p. 149°-150° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05001126 |
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| 出典データセット | uspto-grants-1991_03 |
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| ORD ID | ord-35d8c43986d044b590463d0e55aa15d7 |
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| 出典メモ | uspto-grants-1991_03 |
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