Acid-catalyzed reaction of 4-methyl-1,2,4-triazoline-3,5-dione (MeTAD) with substituted benzenes
β Scribed by Gary W. Breton
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- French
- Weight
- 329 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The reaction of 4-methyl-1,2,4-triazoline-3,5-dione (MeTAD) with substituted benzenes under the influence of trifluoroacetic acid catalysis was investigated. Generally, good-to-high yields of 1-arylurazoles resulting from aromatic substitution were obtained. Successful reaction required moderately electronrich aromatics with proper substitution patterns. The reaction was tolerant of functionality on the aromatic ring.
π SIMILAR VOLUMES
## Abstract The title dienophiles attack nopadiene from the less hindered side.
Several 1,3-dienic terpenes of various structural types are attacked by the title dienophile from the less hindered side. The regiospecificity of attack by methyl triazolinedione(MTAD), 1, upon 1,3-conjugated dienes belonging to the [2.2.2Jbicyclooctane or the norbornane families has been shown to o