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Sodium Chloride → 2-Methyl-2-phenyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Chloride | HCID 5234 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 3-Thiophenecarboxaldehyde | HCID 68135 | — |
| 反応物 | 2,5-dimethyl-2-phenyl-3(2H)-furanone | HCID 15086699 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-Methyl-2-phenyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanone | HCID 54318274 | 71.1% |
反応手順
To a solution of 3-thiophenecarboxaldehyde (1.07 g, 9.6 mM) and 2,5-dimethyl-2-phenyl-3(2H)-furanone (1.5 g, 8 mM) in ethanol (50 mL), was added 1N aqueous sodium hydroxide (1.6 mL, 1.6 mM). After the reaction solution was stirred at room temperature for one day, saturated aqueous sodium chloride (400 mL) was added. The aqueous layer was extracted with dichloromethane (3×100 mL). The combined dichloromethane extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give a yellow liquid. The liquid was purified by chromatography (silica gel, pet. ether-ethyl acetate) to afford a yellow solid (1.6 g, 71% yield), m.p. 75°-77° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05001126 |
| 出典データセット | uspto-grants-1991_03 |
| ORD ID | ord-a78c709543a540b3a961308bb590019e |
| 出典メモ | uspto-grants-1991_03 |