Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51795Generated: October 29, 2026

Water → (4-Bromo-2-methyl-benzyloxy)-trimethylsilane

https://huagongshe.com/reaction/51795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant(4-Bromo-2-methylphenyl)methanolHCID 22280088—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-2-methyl-benzyloxy)-trimethylsilaneHCID 22568853—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of (4-bromo-2-methyl-phenyl)-methanol (Intermediate 133, 500.0 mg, 2.48 mmols), in 10 mL THF was added triethylamine (374.0 mg, 3.70 mmols) and chlorotrimethylsilane (297.0 mg, 2.70 mmols). The resulting solution was stirred for 17 hours at 25° C. and then treated with H2O and extracted with Et2O. The combined organic layers were washed with H2O; 10% aqueous HCl, saturated NaHCO3, and saturated NaCl before being dried (MgSO4) and concentrated under reduced pressure. The title compound, 550.0 mg (81%), was isolated by column chromatography (5% EtOAc-hexanes) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713647B2
Source datasetuspto-grants-2004_03
ORD IDord-73c9d9b2eb2d41caa0a2a84708d3686e
Source noteuspto-grants-2004_03