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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779742Generated: October 27, 2026

Ethyl bromoacetate → ethyl 2-(2-nitro-1H-imidazol-1-yl)acetate

https://huagongshe.com/reaction/1779742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant2-NitroimidazoleHCID 10701—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl acetate hexaneHCID 21226206—
SolventAcetoneHCID 180—
Productethyl 2-(2-nitro-1H-imidazol-1-yl)acetateHCID 327541—

Reaction Steps

To a mixture of 2-nitroimidazole (8 g, 70 mmol) and dry K2CO3 (9.7 g, 70 mmol) in acetone (100 mL) was added ethyl bromoacetate (11.6 g, 70 mmol). The suspension was stirred under N2 atmosphere for 48 h. TLC (silica gel, 40% hexane-ethyl acetate) showed a single UV-visible spot with Rf =0.55. The suspension was filtered and solid was washed with acetone (3×50 mL). The filtrate and the washings were combined and evaporated on a rotary evaporator to afford a thick yellow oil. Yield: 13.9 (99%). MS: 217 (M+NH4)+, 200 (M+H)+. 1H NMR (CDCl3) ε 1.30 (t, 3H, OCH2CH3), 4.26 (q, 2H, OCH2CH3), 5.12 (s, 2H, CH2CO), 7.09 and 7.21 (s, 2H, imidazolyl-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05627286
Source datasetuspto-grants-1997_05
ORD IDord-11604981d96544bdba859a2c518b5082
Source noteuspto-grants-1997_05