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HRID 8201作成日:2026年10月23日

Sodium Hydroxide → 4-Hydroxy-3-(3-methoxy-phenyl)-butyric acid benzhydrylidene-hydrazide

https://huagongshe.com/ja/reaction/8201

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物DiphenylmethylidenehydrazineHCID 79304—
反応物TrimethylaluminumHCID 16682925—
反応物4-(3-Methoxyphenyl)oxolan-2-oneHCID 69364637—
溶媒DichloromethaneHCID 6344—
生成物4-Hydroxy-3-(3-methoxy-phenyl)-butyric acid benzhydrylidene-hydrazideHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087626B2
出典データセットuspto-grants-2006_08
ORD IDord-9cd95b0817f941b7980e1a771dfd5afc
出典メモuspto-grants-2006_08