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HRID 546770作成日:2026年10月27日

Dimethyl Sulfoxide → Ethyl (2-fluoro-3-methylphenyl)acetate

https://huagongshe.com/reaction/546770

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物Sodium IodideHCID 5238—
反応物Ethyl AcetateHCID 8857—
反応物Sodium CyanideHCID 8929—
反応物Benzene, 1-(bromomethyl)-2-fluoro-3-methyl-HCID 519062—
溶媒WaterHCID 962—
生成物Ethyl (2-fluoro-3-methylphenyl)acetateHCID 55268648—

反応条件

温度60 °C

反応手順

A mixture of 2-fluoro-3-methylbenzyl bromide (2.0 g), sodium cyanide (2.41 g), sodium iodide (148 mg) and DMSO (10 ml) was stirred at 60° C. for two hours. Water and ethyl acetate were added to the reaction solution, and the organic layer was separated. The organic layer was washed with brine. The resulting organic layer was dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure. 5 N hydrochloric acid (15 ml) was added to the residue, and the reaction solution was heated at 110° C. for 22 hours. The reaction solution was brought to room temperature. Chloroform was added and the organic layer was separated. The organic layer was concentrated under reduced pressure. Saturated hydrogen chloride-ethanol (15 ml) was added to the residue, and the reaction solution was stirred at 85° C. for four hours. The reaction solution was concentrated under reduced pressure, and then diluted with ethyl acetate and washed with saturated sodium bicarbonate water and then with brine. The resulting organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain the title compound (1.1 g). The property values of the compound are as follows.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07935815B2
出典データセットuspto-grants-2011_05
ORD IDord-761e8e3a9c9744d3a9e703a7e319a9f4
出典メモuspto-grants-2011_05