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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339579Generated: October 29, 2026

4-Hydroxybenzaldehyde → 4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehyde

https://huagongshe.com/reaction/339579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
SolventAcetonitrileHCID 6342—
Product4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehydeHCID 5795610179.5%

Reaction Steps

To a stirred suspension of 4-hydroxybenzaldehyde (0.500 g, 4.012 mmol) and anhydrous potassium carbonate (0.833 g, 6.019 mmol) in dry MeCN (15 ml) at room temperature was added 2-bromo-1-tert-butyldimethylsiloxyethane (83%, 1.730 g, 6.019 mmol), and the reaction mixture was heated under reflux for 20.5 h. Water (25 ml) was added and the reaction mixture was extracted with Et2O (4×25 ml). The combined organic extracts were washed with brine (50 ml), dried (Na2SO4), and the solvent was removed under reduced pressure to give a pale yellow oil that was purified by flash chromatography (3:1 Hexane/Et2O) to give the title compound (0.895 g, 79.5%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895313B2
Source datasetuspto-grants-2014_11
ORD IDord-4ebaf48e08e24b8d90213a9d59741425
Source noteuspto-grants-2014_11