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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | HCID 12639347 | HCID 12639347 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-NITRO-BENZYL)-1H-IMIDAZOLE | HCID 10442861 | 51.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604029B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-7fd81ecaea744fad8fd06a73f2da3724 |
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| Source note | uspto-grants-2013_12 |
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