Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910817Generated: November 2, 2026

Aminoacetaldehyde dimethyl acetal → 2-(4-NITRO-BENZYL)-1H-IMIDAZOLE

https://huagongshe.com/reaction/1910817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantHCID 12639347HCID 12639347—
SolventEthanolHCID 702—
Product2-(4-NITRO-BENZYL)-1H-IMIDAZOLEHCID 1044286151.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 2-(4-nitrophenyl)-acetimidate hydrochloride (3.5 g, 14.3 mmol) in ethanol (15 mL) was added amino acetaldehyde dimethyl acetal (1.87 mL, 17.2 mmol) and the reaction heated at reflux for 18 h. The reaction mixture was concentrated which was mixed with 2N hydrochloric acid (30 mL) and heated to 60° C. for 18 h. The solvent was evaporated, diluted with water and extracted with ethyl acetate. The organic layer was separated, the aqueous layer basified with sodium carbonate and extracted with chloroform (×2). The combined chloroform extracts was dried over sodium sulfate, filtered and evaporated under reduced pressure to obtain 2-(4-nitro-benzyl)-1H-imidazole (1.5 g, 51%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604029B2
Source datasetuspto-grants-2013_12
ORD IDord-7fd81ecaea744fad8fd06a73f2da3724
Source noteuspto-grants-2013_12