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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 2,2-Bis(4-bromophenyl)hexafluoropropane | HCID 13878551 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,2-Bis(4-trimethylsilylphenyl)hexafluoropropane | HCID 13878552 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04722985 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-c8ad3021517e47849a4ef0618fa4b5f1 |
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| Source note | uspto-grants-1988_02 |
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