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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3903Generated: October 23, 2026

Chlorotrimethylsilane → 2,2-Bis(4-trimethylsilylphenyl)hexafluoropropane

https://huagongshe.com/en/reaction/3903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2,2-Bis(4-bromophenyl)hexafluoropropaneHCID 13878551—
ReactantAcetone cardiceHCID 18522661—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2,2-Bis(4-trimethylsilylphenyl)hexafluoropropaneHCID 13878552—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4.62 g (0.1 mole) 2,2-bis(4-bromophenyl)hexafluoropropane in 75 ml of anhydrous tetrahydrofuran was added dropwise 28 ml (0.4 moles) of a 1.4 molar solution of n-butyllithium in hexane while the reaction mixture was cooled in a dry ice-acetone slush. The reaction mixture was stirred for one half hour at -78° C. A dropwise addition of chlorotrimethylsilane (5 ml, 0.04 moles) was then made to the reaction mixture at -78° C. The stirring slurry was allowed to come to ambient temperature over 16 hours. To the reaction mixture was added 100 ml hexane. The organic layer was washed with 2×150 ml saturated sodium chloride solution and 2×150 ml water. The organic layer was dried, filtered, and concentrated to yield the white crystalline product 2,2-bis(4-trimethylsilylphenyl)hexafluoropropane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04722985
Source datasetuspto-grants-1988_02
ORD IDord-c8ad3021517e47849a4ef0618fa4b5f1
Source noteuspto-grants-1988_02