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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloro(chloromethyl)[bis(4-fluorophenyl)]silane | HCID 13392398 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Potassium imidazole | HCID 67086713 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [bis(4-Fluorophenyl)](1H-imidazol-1-ylmethyl)silane | HCID 123558487 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04530922 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-d0061b22668941c1829a4bfb896d9772 |
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| Source note | uspto-grants-1985_07 |
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