Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980140Generated: October 29, 2026

Imidazole → 4-(2-(1H-imidazol-1-yl)ethoxy)benzamide

https://huagongshe.com/reaction/980140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium hydrideHCID 24758—
Reactant4-(2-Chloroethoxy)benzamideHCID 13569171—
SolventDimethylformamideHCID 6228—
Product4-(2-(1H-imidazol-1-yl)ethoxy)benzamideHCID 1356917750.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydride (14.4 g, 50% suspension in mineral oil) was added cautiously to a stirred and cooled solution of imidazole (20.4 g) in dry N,N-dimethylformamide (100 ml). After the initial vigorous reaction had subsided the mixture was heated to 100° C. for 10 minutes and then stirred at room temperature for a further 1 hour. A solution of 4-(2-chloroethoxy)benzamide (60.0 g) in the minimum volume of N,N-dimethylformamide was added and the mixture was heated at 100° C. for 5.5 hours. The solvent was evaporated and the residue was poured into water. The mixture was extracted several times with chloroform and the combined chloroform extracts were dried (MgSO4) and evaporated to give a mixture of oil and solid. The mixture was triturated with ether and the solid was collected and crystallised from a mixture of methanol and ethyl acetate to give 1-[2-(4-carbamoyl phenoxy)ethyl]imidazole (35.2 g), m.p. 148°-149° C. Found: C, 62.25; H, 5.61; N, 18.54. C12H13N3O2 requires C, 62.32; H, 5.67; N, 18.17%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636500
Source datasetuspto-grants-1987_01
ORD IDord-6562182901ca4904af4a1c1351837531
Source noteuspto-grants-1987_01