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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443758Generated: November 1, 2026

Triethylamine → (4-(5-Bromo-2-chlorobenzyl)phenoxy)(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/1443758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-((5-Bromo-2-chlorophenyl)methyl)phenolHCID 57423751—
SolventDichloromethaneHCID 6344—
Product(4-(5-Bromo-2-chlorobenzyl)phenoxy)(tert-butyl)dimethylsilaneHCID 59747702—

Reaction Steps

A solution of 13.9 g 4-(5-bromo-2-chloro-benzyl)-phenol in 140 mL dichloromethane is cooled in an ice bath. Then 7.54 g tert-butyidimethylsilyl chloride in 20 mL dichloromethane are added followed by 9.8 mL triethylamine and 0.5 g dimethylaminopyridine. The resultant solution is stirred for 16 h at ambient temperature and then diluted with 100 mL dichloromethane. The organic phase is washed twice with aqueous 1 M hydrochloric acid and once with aqueous sodium hydrogen carbonate solution and then dried over sodium sulfate. After the solvent is removed, the residue is filtered through silica gel (cyclohexane/ethyl acetate 100:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662790B2
Source datasetuspto-grants-2010_02
ORD IDord-b4722088b77046d89e0d05a5956ca61f
Source noteuspto-grants-2010_02