Synthesis of 4-nitro-1-(trialkylsilylalkyl)imidazoles
✍ Scribed by Földeák, Sándor ;Molnár, Mária ;L??kös, Magdalena
- Book ID
- 102366343
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 129 KB
- Volume
- 1994
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
1‐(2‐Hydroxyethyl)‐2‐methyl‐5‐nitroimidazole (1) reacts with haloalkyltrialkylsilanes [Hal(CH~2~)~n~SiMe~2~R] to give 4‐nitroimidazole derivatives 3 and acetaldehyde. This process involves at least two reaction steps, N‐alkyl quaternization and elimination of the hydroxyethyl group. magnified image
📜 SIMILAR VOLUMES
In the title compound, C 10 H 8 N 4 O 4 , two planar fragments, viz. the imidazole and nitrophenyl rings, are tilted at a dihedral of 57.89 (7) . The nitro groups are twisted with respect to the neighbouring ring planes; the dihedral angle is 7.0 (3) for imidazole and 9.68 (8) for benzene. The cryst
The first syntheses of 4(5)-nitro-IH-imidazole-5(4)-carbonitrile, its 2-methyl derivative and salts of both compounds with DBU have been described. The carbonitriles have been obtained by a treatment of 1,4-dinitroimidazoles with potassium cyanide in aqueous methanol solution.