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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806873Generated: October 31, 2026

Potassium Carbonate → 2-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-chloro-benzaldehyde

https://huagongshe.com/reaction/1806873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Chloro-salicylaldehydeHCID 12481—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-chloro-benzaldehydeHCID 5756591694.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

Step A To a solution of 5-chlorosalicylaldehyde (2 g, 12.8 mmol) (Aldrich) in N,N-dimethylformamide (40 mL) was added K2CO3 (5.3 g, 38 mmol), and (2-bromo-ethoxy)-tert-butyl-dimethyl-silane (3.67 g, 15 mmol, Aldrich). The reaction mixture was heated at 60° C. for 18 h. The crude was cooled to room temperature, diluted with ethyl acetate, washed with water, brine. The organic layer was separated, concentrated, and the residue was purified by chromatography (EtOAc:Hexanes=1:8, then 1:4) to give 2-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-chloro-benzaldehyde as a brown oil (Yield 3.8 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-6c6c6e3a0db04605b2fea5e748b21030
Source noteuspto-grants-2013_01