関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Diphenylmethylidenehydrazine | HCID 79304 | — |
| 反応物 | Trimethylaluminum | HCID 16682925 | — |
| 反応物 | 4-(3-Methoxyphenyl)oxolan-2-one | HCID 69364637 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-Hydroxy-3-(3-methoxy-phenyl)-butyric acid benzhydrylidene-hydrazide | HCID 86592621 | — |
反応手順
Trimethylaluminum (12 mL, 2 M in hexane, 24 mmol) is added dropwise to a solution of benzophenone hydrazone (1.57 g, 8 mmol) in dichloromethane (20 mL) at room temperature and under nitrogen. After the mixture is stirred for 30 min, 4-(3-methoxy-phenyl)-dihydro-furan-2-one, (1.54 g, 8 mmol) in dichloromethane (5 mL) is added. The mixture is refluxed for 5 h cooled to room temperature and diluted with dichloromethane (30 mL). The mixture is treated with 4 N sodium hydroxide (30 mL) and stirred one hour. The organic layer is separated, washed with brine and, dried over magnesium sulfate. The mixture is filtered, concentrated in vacuo and chromatographed on SiO2 (2% methanol/dichloromethane) to yield the title compound, 2.25 g (73%) as a pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07087626B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-9cd95b0817f941b7980e1a771dfd5afc |
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| 出典メモ | uspto-grants-2006_08 |
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