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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372903Generated: October 26, 2026

Dichloromethane → 2-[2-[[Dimethyl(1,1,2-trimethylpropyl)silyl]oxy]ethyl]benzene bromide

https://huagongshe.com/reaction/2372903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantChloro(hexyl)dimethylsilaneHCID 2733540—
Reactant2-(3-Bromophenyl)ethan-1-olHCID 2734090—
SolventHexaneHCID 8058—
Product2-[2-[[Dimethyl(1,1,2-trimethylpropyl)silyl]oxy]ethyl]benzene bromideHCID 1987537695%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Bromophenethyl alcohol (46.0 g, 228.78 mmol) was combined with dimethylaminopyridine (6.99 g, 57.19 mmol) and triethylamine (34.73 g, 343.17 mmol) in anhydrous CH2Cl2 (200 mL) and cooled to 0° C. Dimethylhexylsilyl chloride (44.18 g, 247.08 mmol) was added dropwise over ten minutes, then the reaction mixture was warmed to room temperature and stirred for sixteen hours. The reaction mixture was diluted with hexane (800 mL) and filtered. The filtrate was concentrated and the residue was partitioned between ether (800 mL) and 0.3N aqueous HCl (2 times with 400 mL), saturated aqueous NaHCO3 (400 mL), dried (MgSO4) and concentrated. The crude liquid was chromatographed on a silica gel column and eluted with 20% ether in hexane to give title compound (74.45 g, 95%) as a clear liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100889
Source datasetuspto-grants-1992_03
ORD IDord-2f9ae7d2c2da49deb42afa0f14d4e874
Source noteuspto-grants-1992_03