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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901123Generated: October 31, 2026

Water → 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde

https://huagongshe.com/reaction/901123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant[1-(triphenylmethyl)-1H-imidazol-4-yl]methanolHCID 382182—
SolventDimethyl SulfoxideHCID 679—
Product1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—

Reaction Conditions

Temperature110 °C

Reaction Steps

The product from Step 8.a. (2.04 g, 6.00 mmol) was suspended in DMSO (10.0 ml) and Et3N (3.34 ml, 24.0 mmol) and SO3-pyridine complex (2.39 g, 15.0 mmol) were added at room temperature. The mixture was warmed at about 110° C. for about 1 hour and then allowed to cool. The mixture was poured into 150 ml H2O and the product was filtered off. The residue was treated with saturated NaHCO3 solution (50 ml) and extracted 2×100 ml CH2Cl2. The combined CH2Cl2 layers were washed with 5% citric acid solution (100 ml), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was crystallized from MeOH and H2O. Yield=1.08 g (53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361656B2
Source datasetuspto-grants-2008_04
ORD IDord-2f7bebf242b043158f96d189fb9a9a5c
Source noteuspto-grants-2008_04