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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371314Generated: October 27, 2026

Chloro(chloromethyl)[bis(4-fluorophenyl)]silane → [bis(4-Fluorophenyl)](1H-imidazol-1-ylmethyl)silane

https://huagongshe.com/reaction/371314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloro(chloromethyl)[bis(4-fluorophenyl)]silaneHCID 13392398—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantPotassium imidazoleHCID 67086713—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product[bis(4-Fluorophenyl)](1H-imidazol-1-ylmethyl)silaneHCID 123558487—

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 3.0 g (9.9 mmol) of bis(4-fluorophenyl)chlorochloromethylsilane and 50 mg of tetrabutylammonium hydrogen sulfate in 10 ml of toluene is added 2.2 g (20.5 mmol) of potassium imidazole. The resulting exotherm is controlled by cooling with ice-water. Th solution is heated at reflux for 5 hours and then was cooled to -70° C. A solution of 10.5 ml (10.5 mmol) of diisobutylaluminum hydride (1.0 molar) in tetrahydrofuran is then added dropwise, and the reaction is warmed to room temperature and quenched by dropwise addition of saturated aqueous ammonium chloride. The solution is diluted with methylene chloride and washed three times with water and once with brine. Drying over magnesium sulfate and removal of solvent gives a viscous oil which is triturated with ether to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04530922
Source datasetuspto-grants-1985_07
ORD IDord-d0061b22668941c1829a4bfb896d9772
Source noteuspto-grants-1985_07