Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728130Generated: November 1, 2026

Potassium Carbonate → 2-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-iodo-3-methoxy-benzaldehyde

https://huagongshe.com/reaction/1728130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzaldehyde, 4-hydroxy-3-iodo-5-methoxy-HCID 79499—
Reactant(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 3608067—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-[2-(Tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-iodo-3-methoxy-benzaldehydeHCID 5756595496%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-iodovanillin (10 g, 35.9 mmol) (Aldrich) in N,N-dimethylformamide (150 mL) was added anhydrous K2CO3 (14.9 g, 108 mmol), and (2-bromo-ethoxy)-tert-butyl-dimethyl-silane (10.3 g, 43 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, dried over MgSO4, concentrated, and purified by chromatography to give 2-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-iodo-3-methoxy-benzaldehyde as a yellow oil (Yield 15 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-4348e8e7fe684d42b17a268558ed48fa
Source noteuspto-grants-2009_02