HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075970Generated: October 26, 2026
Diazomethane → Ethanone, 1-(1-methyl-2-nitro-1H-imidazol-5-yl)-
https://huagongshe.com/reaction/1075970
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | 1-Methyl-2-nitro-1H-imidazole-5-carboxaldehyde | HCID 100390 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethanone, 1-(1-methyl-2-nitro-1H-imidazol-5-yl)- | HCID 21503737 | — |
Reaction Steps
To a solution of 0.70 g. of 1-methyl-2-nitro-5-imidazolecarboxaldehyde in 180 ml. of diethyl ether, a solution of 0.43 g. of diazomethane in 86 ml. of diethyl ether is added under cooling at about 0° C. After standing at room temperature for 7 days, the reaction mixture is filtered and then evaporated to dryness. The residue (0.60 g.), dissolved, in 6 ml. of chloroform, is chromatographed on 6 plates of silica gel, eluting with a 9:1 (v/v) chloroform:methanol mixture, and TLC spots are visualized under U.V. light. The silica gel, which corresponds to an Rf value from 0.64 up to 0.76 is collected and extracted with methanol. From this solution, after filtration and concentration, 0.065 g. of 5-acetyl-1-methyl-2-nitroimidazole is obtained, m.p. 81°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03954789 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-a72756c870e04875932f2d468ce98da2 |
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| Source note | uspto-grants-1976_05 |
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