Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51299Generated: October 26, 2026

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

https://huagongshe.com/reaction/51299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant1H-Imidazole-4-carbaldehydeHCID 76428—
SolventDimethylformamideHCID 6228—
Product1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—

Reaction Steps

A solution of trityl chloride (9.5 g, 34.3 mmol) in N,N-dimethylformamide (50 ml) was added dropwise to an ice-cooled solution of imidazole-4-carboxaldehyde (3 g, 31.2 mmol) and triethylamine (17 ml, 125 mmol) in N,N-dimethylformamide (30 ml) and the solution was stirred for 2 hours. The reaction was then allowed to warm to room temperature, and was stirred for a further 18 hours. Water (200 ml) was added, and the resulting pink solid was collected and dried, then dissolved in dichloromethane (200 ml). The resulting solution was washed with water (2×100 ml), dried (MgSO4) and evaporated under reduced pressure. The product was recrystallised from ethanol to afford the title compound as a solid, 7.8 g. 1H-NMR (CDCl3, 400 MHz) δ: 7.06 (m, 6H), 7.32 (m, 9H), 7.48 (s, 1H), 7.58 (s, 1H), 9.82 (s, 1H). Microanalysis found: C, 81.54; H, 5.37; N, 8.24. C23H18N2O requires C, 81.63; H, 5.36; N, 8.28%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713496B2
Source datasetuspto-grants-2004_03
ORD IDord-7e4a9f9166434d7ba8d06a2ed98ab35d
Source noteuspto-grants-2004_03