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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400623Generated: October 26, 2026

Vinylidene fluoride → (1-Fluorovinyl)dimethylphenylsilane

https://huagongshe.com/reaction/400623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinylidene fluorideHCID 6369—
ReactantChlorodimethylphenylsilaneHCID 13029—
ReactantLithiumHCID 3028194—
ReactantHCID 178506968HCID 178506968—
SolventTetrahydrofuranHCID 8028—
Product(1-Fluorovinyl)dimethylphenylsilaneHCID 60026366—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741897B2
Source datasetuspto-grants-2014_06
ORD IDord-22e73bbb78f740d786a181cd35b9046a
Source noteuspto-grants-2014_06