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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738708Generated: October 31, 2026

4-Hydroxybenzaldehyde → 4-[(1-Trityl-4-imidazolyl)methoxy]benzaldehyde

https://huagongshe.com/reaction/1738708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Chloromethyl)-1-trityl-1H-imidazoleHCID 2763176—
SolventDimethylformamideHCID 6228—
Product4-[(1-Trityl-4-imidazolyl)methoxy]benzaldehydeHCID 1542903751.8%

Reaction Steps

1.22 g of p-hydroxybenzaldehyde and 4.08 g of 4-chloromethyl-1-tritylimidazole were dissolved in 40 ml of N,N-dimethylformamide, followed by adding 1.66 g of anhydrous potassium carbonate and subsequently stirring at room temperature for 40 hours. The thus prepared reaction solution were partitioned between water and benzene, and the resulting organic layer was concentrated to dryness. The resulting residue was purified by subjecting it to silica gel column chromatography using chloroform as an elution solvent, and the thus purified product was crystallized from a n-hexane/benzene solvent system. In this way, 2.3 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962695
Source datasetuspto-grants-1999_10
ORD IDord-4ab3b6ab2e144e868577125647162fe5
Source noteuspto-grants-1999_10