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HRID 970763作成日:2026年10月24日

Water → 3-Methyl-1-phenyl-buten-3-ol

https://huagongshe.com/ja/reaction/970763

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Diethyl EtherHCID 3283—
反応物Ammonium ChlorideHCID 25517—
反応物Ethyl CinnamateHCID 637758—
反応物HCID 178418373HCID 178418373—
生成物3-Methyl-1-phenyl-buten-3-olHCID 92677—

反応手順

To a cooled (−10 to −5° C.) 165 mL of 3 M solution of methyl magnesium iodide in ether was added dropwise a solution of ethyl trans-cinnamate (25.0 g) in 200 mL of anhydrous ether. The reaction was warmed to room temperature and stirred overnight. The mixture was then heated up to 33° C. under reflux for two hours and cooled to 0° C. A white solid was formed during cooling and water (105 mL) was gradually added to dissolve the white precipitate followed by an additional 245 mL of saturated aqueous ammonium chloride solution. The mixture was then stirred until the solids were completely dissolved and extracted with 100 mL of ether three times. The combined extract was washed with 100 mL of water, dried over anhydrous sodium sulfate and filtered. The solvent was evaporated to give 22.1 g of the desired 4-phenyl-2-methyl-3-buten-2-ol as an oil which was used in the next step without further purification. 1H NMR (CDCl3, 300 MHz), δ(ppm) 7.41 (m, 5H), 6.58 (d, 1H), 6.34 (d, 1H), 1.41 (broad s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07312247B2
出典データセットuspto-grants-2007_12
ORD IDord-478ceff5298b4dfcb5dd6ea99134a591
出典メモuspto-grants-2007_12