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HRID 2073923作成日:2026年10月25日

Phenolate Sodium → Silafluofen

https://huagongshe.com/reaction/2073923

反応式

関与物質

役割名称HCID仕込み量
反応物Phenolate SodiumHCID 4445035—
反応物1-((3-(3-Chloro-4-fluorophenyl)propyl)dimethylsilanyl)-4-ethoxybenzeneHCID 10948112—
触媒Cuprous chlorideHCID 62652—
溶媒TetraglymeHCID 8925—
生成物SilafluofenHCID 9243044%

反応条件

温度90 °C

反応手順

A mixture of 456.2 g (1.30 mol) of (4-ethoxyphenyl)-(dimethyl)-(3-(3-chloro-4-fluorophenyl)propyl)silane, 232.2 g (2.00 mol) of sodium phenolate, 13 g of copper(I) chloride and 500 ml of tetraglyme was heated to 240°-255° C. for 1.5 h. After cooling the reaction mixture to 90° C., a larger part of the solvent was removed by distillation at 90°-140° C. internal temperature and 0.4 Torr (about 400 g). The crude product was then stirred at room temperature with 500 ml of 2N sodium hydroxide solution and extracted twice using 800 ml of hexane each time. The organic extracts were washed five times with 300 ml of water each time, dried over sodium sulfate and evaporated. The crude product thus obtained (486.1 g/92%) was distilled over a 50 cm split tube column. 233 g (44%) of (4-ethoxyphenyl)-(dimethyl)-(3-(4-fluoro-3-phenoxyphenyl)propyl)silane were obtained as a colorless oil of b.p.0.04 =208°-212° C., the purity of which was determined to be 95.2% by gas chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04920212
出典データセットuspto-grants-1990_04
ORD IDord-6c80d61f41ee4aac817d0c93a785c085
出典メモuspto-grants-1990_04