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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217788Generated: October 30, 2026

Triethylamine → [2-(4-Bromophenyl)ethoxy](tert-butyl)dimethylsilane

https://huagongshe.com/reaction/217788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-(4-Bromophenyl)ethanolHCID 72851—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product[2-(4-Bromophenyl)ethoxy](tert-butyl)dimethylsilaneHCID 2325450090.1%

Reaction Steps

To a solution of 2-(4-bromophenyl)ethanol (5 g, 25 mmol) in anhydrous dichloromethane (150 mL) was added triethylamine (7.5 g, 75 mmol), DMAP (300 mg, 2.5 mmol) and tert-butyldimethylsilyl chloride (7.5 g, 50 mmol) sequentially. The resulting pale brown solution was stirred at room temperature for overnight. The reaction mixture was extracted with dichloromethane and water three times. The combined organic layers were dried over anhydrous sodiumsulphate, filtered and concentrated in vacuo. The crude product was subjected to column chromatography with PE as eluant to afford the subtitle compound as a brown oil (7.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198285B2
Source datasetuspto-grants-2012_06
ORD IDord-be5cf02a0555476c9cc9545c1f71dff9
Source noteuspto-grants-2012_06