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HRID 400623作成日:2026年10月25日

Vinylidene fluoride → (1-Fluorovinyl)dimethylphenylsilane

https://huagongshe.com/reaction/400623

反応式

関与物質

役割名称HCID仕込み量
反応物Vinylidene fluorideHCID 6369—
反応物ChlorodimethylphenylsilaneHCID 13029—
反応物LithiumHCID 3028194—
反応物HCID 178506968HCID 178506968—
溶媒TetrahydrofuranHCID 8028—
生成物(1-Fluorovinyl)dimethylphenylsilaneHCID 60026366—

反応手順

To a suspension of 4.4 g of lithium wire cut into small pieces in 200 mL of anhydrous THF stirred under argon and cooled on ice (internal temperature <10° C.) was added dimethylphenyl-chlorosilane in 5 mL portions over 1 hour. The deep red color of the silyl lithium reagent appeared after approximately 0.75 hour. The mixture was stirred on ice for an additional 5 hours (internal temperature remained between 5° C. and 10° C.). The mixture was cooled on a dry ice/acetone bath and 1,1-difluoroethylene was introduced by filling a balloon connected to the reaction mixture and the reagent cylinder using a three-way valve. The balloon was filled with 1,1-difluoroethylene and emptied into the reaction mixture 10 times. The mixture was allowed to warm to room temperature (effervescence observed, probably from unreacted 1,1-difluoroethylene). The mixture was diluted with 200 mL of hexanes and filtered through a cotton wool plug. The filtrate was washed with water, dried, filtered, and concentrated in vacuo. Four fractional distillations under vacuum through a Vigreux column gave 4.6 g of product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741897B2
出典データセットuspto-grants-2014_06
ORD IDord-22e73bbb78f740d786a181cd35b9046a
出典メモuspto-grants-2014_06