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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450928Generated: November 2, 2026

Imidazole → Tert-butyl[4-(iodomethyl)phenoxy]dimethylsilane

https://huagongshe.com/reaction/450928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-((Tert-butyldimethylsilyl)oxy)phenyl)methanolHCID 10014460—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl[4-(iodomethyl)phenoxy]dimethylsilaneHCID 2176023141%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triphenyl phosphine (1.32 g, 5.03 mmol), imidazole (370 mg, 5.47 mmol) and iodine (1.16 g, 4.61 mmol) were added to an ice-cooled solution of 4-(tert-butyldimethylsilyloxy)benzyl alcohol [(1 g, 4.19 mmol), Tet. Lett. (2004), 45, 9617] in tetrahydrofuran (50 mL) and the mixture was stirred at 0° C. for 10 minutes and room temperature for 30 minutes. The reaction mixture was then concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic layer was separated, dried over magnesium sulfate and concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with pentane, afforded the title compound in 41% yield, 600 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486992B2
Source datasetuspto-grants-2013_07
ORD IDord-e2cfa20cb8ac4e59ad06daf5a2981dbc
Source noteuspto-grants-2013_07