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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23710Generated: October 26, 2026

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

https://huagongshe.com/reaction/23710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantHexaneHCID 8058—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantBenzaldehyde, 4-(2-hydroxyethoxy)-HCID 89178—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(2-(Tert-butyldimethylsilyloxy)ethoxy)benzaldehydeHCID 5795610149.9%

Reaction Steps

To 4-(2-hydroxyethoxy)benzaldehyde (commercial, 0.5 g, 3 mmol) dissolved in DMF (10 mL) is added imidazole (0.4 g, 6 mmol) and tert-butyldimethylsilylchloride (0.53 g, 3.5 mmol). Reaction mixture is stirred for 20 h. at room temperature. TLC analysis (hexane:ethyl acetate,7:3) shows small amounts of unreacted starting material. Additional tert-butyldimethylsilylchloride (0.25 g, 1 mmol) is added and stirring continued for 16 h. The reaction is quenched with saturated aqueous ammonium chloride (20 mL) and diluted further with ethyl ether (20 mL). Aqueous layer is separated and extracted thrice with ether (10 mL). Combined organics dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue is purified by flash chromatography on silica gel using a gradient of 2% to 5% ethyl acetate in hexanes to provide 0.42 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852731B2
Source datasetuspto-grants-2005_02
ORD IDord-80c3f0ea60a240ea855be153730b5b6d
Source noteuspto-grants-2005_02