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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400545Generated: October 29, 2026

Imidazole → [4-(Bromomethyl)-phenoxy][tris(1-methylethyl)]silane

https://huagongshe.com/reaction/2400545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriphenylphosphineHCID 11776—
ReactantTriphenylphosphine OxideHCID 13097—
ReactantBromineHCID 24408—
Reactant(4-((Triisopropylsilyl)oxy)phenyl)methanolHCID 59504706—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product[4-(Bromomethyl)-phenoxy][tris(1-methylethyl)]silaneHCID 44134296—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (4-{[tris(1-methylethyl)silyl]oxy}phenyl)methanol (Step 2, 1.0 g, 3.56 mmol) in diethyl ether (20 mL) and acetonitrile (7.5 mL) was added triphenylphosphine (0.94 g, 3.57 mmol) and imidazole (243 mg, 3.57 mmol). After being cooled to 0° C., a solution of bromine (184 μL, 3.56 mmol) in diethyl ether (2.5 mL) was added dropwise. The reaction mixture was stirred at rt over night. Then water was added, and it was extracted with ethyl acetate. The organic extract was washed with water and brine, dried over anhydrous magnesium sulfate and filtered. After evaporation of the solvent, the crude material was treated with pentane. Precipitated triphenylphosphine oxide (TPPO) was removed by filtration. The solvent was evaporated in vacuo. The product thus obtained (1.42 g) still contained some TPPO (as judged by tlc) but was used for subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796253B2
Source datasetuspto-grants-2014_08
ORD IDord-9ef4a0b986f84a4bb9b0848133024da8
Source noteuspto-grants-2014_08