Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899687Generated: October 29, 2026

Imidazole → ethyl 2-(1H-imidazol-1-yl)acetate

https://huagongshe.com/reaction/899687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Productethyl 2-(1H-imidazol-1-yl)acetateHCID 379850165.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. suspension of NaH (60% in mineral oil, 658 mg, 16.5 mmol) in THF (20 mL) under nitrogen was slowly added a solution of imidazole (1.03 g, 15.1 mmol) in THF (20 mL). The resulting suspension was stirred at 0° C. for 15 minutes, then ethyl bromoacetate (2.2 mL, 20 mmol) was added. The reaction was stirred at room temperature for 4.5 hours, then was diluted with H2O (25 mL). The THF was evaporated under reduced pressure and the remaining aqueous solution was extracted with CH2Cl2 (25 mL×3). The combined organic solution was dried (Na2SO4), filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica (CH2Cl2/MeOH, 19:1) gave the ester as a yellow liquid (1.52 g, 9.87 mmol, 65%). 1H NMR (CDCl3) δ 1.28 (t, 3H, J=7.1 Hz), 4.24 (q, 2H, J=7.1 Hz), 4.68 (s, 2H), 6.95 (s, 1H), 7.09 (s, 1H), 7.50 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354932B2
Source datasetuspto-grants-2008_04
ORD IDord-08277945a4604328be3832bed4c359b4
Source noteuspto-grants-2008_04