HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212319Generated: November 2, 2026
Imidazole → tert-Butyl-(3,5-dibromobenzyloxy)diphenylsilane
https://huagongshe.com/reaction/2212319
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | (3,5-Dibromophenyl)methanol | HCID 7009423 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | tert-Butyl-(3,5-dibromobenzyloxy)diphenylsilane | HCID 21964571 | 94.4% |
Reaction Steps
With stirring, imidazole (1.1 g, 16.0 mmol) is added to a solution of 3,5-dibromobenzyl alcohol (2.8 g, 10.5 mmol) in absolute DMF (20 ml), and the mixture is cooled to 0° C. tert-Butyldiphenylsilyl chloride (3.3 ml, 17.8 mmol) is added dropwise to the reaction solution, which is then stirred at 0° C. for 2 h. The mixture is then warmed to RT and stirred for another 2 h. The reaction mixture is diluted with ethyl acetate (20 ml) and extracted with a semisaturated aqueous NH4Cl solution (20 ml). The organic phase is dried over MgSO4, filtered off and concentrated under reduced pressure. Further purification is carried out by chromatography [PE/EA (99:1)] on a silica gel column. This gives the title compound (5.0 g) as a colorless solid. TLC, silica gel (glass plates), [petroleum ether/ethyl acetate (99:1)], Rf=0.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101911B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-b61e584ea3d64e6aaebcf1e04f10c912 |
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| Source note | uspto-grants-2006_09 |
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