Addendum to synthesis of some 2-oxo-4-aryl-5-carbethozy-6-trifluoromethyl-1,2,3,4-tetrahydropyrimidines
- Publisher
- Elsevier Science
- Year
- 1955
- Tongue
- English
- Weight
- 36 KB
- Volume
- 259
- Category
- Article
- ISSN
- 0016-0032
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β¦ Synopsis
Further proof of structure of 2-oxo-4-(3,4-diethoxyphenyl)-5-carbethoxy-6-trifluoromethyl-l,2,3,4-tetrahydropyrimidine was obtained by comparison of the infrared spectrum* of the compound with that of the 6-methyl analog. The spectra are identical except that a strong band for the C-F bond was found at 8.23 and 8.41 microns in the trifluoromethyl derivative.
More extensive investigation of the ultraviolet absorption spectra of the two compounds indicated the presence of a second absorption peak at 233 millimicrons (density 0.823) for the trifluoromethyl derivative. This may indicate that the compound exists in the enol form in absolute ethanol.
These comparisons of the infrared spectra and of the ultraviolet spectra furnish substantiation of the structure of this trifluoromethyl derivative.
π SIMILAR VOLUMES
Single-crystal X-ray study T = 294 K Mean (C-C) = 0.005 A R factor = 0.052 wR factor = 0.148 Data-to-parameter ratio = 12.7 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.
## Abstract magnified image In the context of our highβthroughput organic synthesis program, we have studied the reactivity of special Ξ²βketo esters toward the Biginelli reaction. We have found that a diethylβ3βoxoglutarate reacts with one molecule of urea and one molecule of aldehyde under solven