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HRID 458125作成日:2026年10月26日

Dimethyl Sulfide → 4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-one

https://huagongshe.com/reaction/458125

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfideHCID 1068—
反応物ChlorotrimethylsilaneHCID 6397—
反応物Mesityl oxideHCID 8858—
反応物2-Bromo-4-fluoroanisoleHCID 136292—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-oneHCID 2228492285%

反応条件

温度-78 °C

反応手順

To a stirred solution of 2-bromo-4-fluoro anisole (3.24 mL, 25 mmol) in anhydrous THF (40 mL) cooled to −78° C. and maintained under argon was added n-butyl lithium (17.2 mL of 1.6 M solution in hexanes, 27.5 mmol). After stirring at −78° C. for 45 minutes, the reaction mixture was treated with a solution of cuprous iodide in dimethyl sulfide (4.76 g in 15 mL, 25 mmol) and stirred for 15 minutes at −78° C. Then chlorotrimethylsilane (6.4 mL, 50 mmol) was added, followed by a solution of mesityl oxide (2.9 mL, 25 mmol) in anhydrous THF (5 mL). The reaction was stirred at −78° C. to −60° C. for 4 hours and then quenched with a saturated solution of ammonium chloride and extracted with three 50 mL portions of methylene chloride. The combined extracts were washed with three 25 mL portions of water, dried over anhydrous sodium sulfate, and concentrated in vacuo to give 4-(5-fluoro-2-methoxyphenyl)-4-methylpentan-2-one as a light brown liquid (85% yield) which was used in the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07189758B2
出典データセットuspto-grants-2007_03
ORD IDord-c8ea7327285d4c5887ed3c45b93c981d
出典メモuspto-grants-2007_03