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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856145Generated: October 29, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-Chloro-4-nitro-1-(oxiran-2-ylmethyl)imidazole

https://huagongshe.com/reaction/856145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2-Chloro-1-(3-chloro-2-hydroxypropyl)-4-nitroimidazoleHCID 23081202—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-nitro-1-(oxiran-2-ylmethyl)imidazoleHCID 2308149311%

Reaction Steps

2-Chloro-1-(3-chloro-2-hydroxypropyl)-4-nitroimidazole prepared in Example 1 (2.04 g, 8.5 mmol) was dissolved in methylene chloride (20 ml), and 1,8-diazabicyclo[5.4.0]-7-undecene (DBU) (2.04 ml, 13.67 mmol) was added to the solution. The resulting mixture was stirred at room temperature overnight. The reaction mixture was washed with 3N hydrochloric acid (20 ml) and a saturated saline solution (20 ml) in this order, dried over sodium sulfate and then filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (methylene chloride/ethyl acetate=20/1) to afford 2-chloro-4-nitro-1-(oxiran-2-ylmethyl)imidazole (190 mg, yield 11%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-d12a79b60ff44a19afddc739a2eb742a
Source noteuspto-grants-2007_08