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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181048Generated: November 2, 2026

Triethylamine → (4-Bromo-3-methylphenoxy)(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/1181048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-Bromo-m-cresolHCID 72857—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(4-Bromo-3-methylphenoxy)(tert-butyl)dimethylsilaneHCID 1798459898.5%

Reaction Steps

A 12 L flask was charged with 4-bromo-3-methyl phenol (428 g, 2.29 mol), CH2Cl2 (7.5 L), triethylamine (480 mL, 3.45 mol), and tert-butyldimethylsilyl chloride (324 g, 2.15 mol). To the solution was added 4-dimethylaminopyridine (15.0 g, 0.123 mol). The reaction mixture was stirred at ambient temperature overnight. The reaction was washed with saturated ammonium chloride (2.2 L) and then DI water (0.9 L). The organic layer was dried (Na2SO4), filtered, and concentrated to crude product (699 g). This material was purified by silica gel chromatography (heptane) to give the title compound (637 g, 98.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282501B2
Source datasetuspto-grants-2007_10
ORD IDord-50cfdbef7ca0445b9cef3bd88b6f464a
Source noteuspto-grants-2007_10