Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255569Generated: November 1, 2026

tert-Butyldimethylsilyl chloride → {[4-(Bromomethyl)phenyl]methoxy}(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/2255569

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Bromomethyl)benzyl alcoholHCID 10330434—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product{[4-(Bromomethyl)phenyl]methoxy}(tert-butyl)dimethylsilaneHCID 1075771171%

Reaction Steps

To a solution of the product of Step A (4.44 g, 22.1 mmol) in CH2Cl2 were added N,N-diisopropylethylamine (1.2 eq.), 4-dimethylaminopyridine (0.1 eq), and tert-butyldimethylsilyl chloride (1.2 eq). The reaction mixture was stirred for 1.5 hours at room temperature, then concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with water, brine, dried (MgSO4), filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluted with 2.5% ethyl acetate/hexane to afford 5.0 g (71%) of the titled product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240938
Source datasetuspto-grants-1993_08
ORD IDord-f462da1e6ab14abeb17108676af51d46
Source noteuspto-grants-1993_08