Ring Closure Reactions of Polychloroazaalkenes
β Scribed by Dr. H.-G. Schmelzer; Dr. E. Degener; Dr. H. Holtschmidt
- Publisher
- John Wiley and Sons
- Year
- 1966
- Tongue
- English
- Weight
- 184 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
β¦ Synopsis
IR spectra of aliphatic isocyanates that are perchlorinated in the a-position indicate that in many cases these compounds exist partly or wholly as N-(a-chloroalky1idene)carbamoyl chlorides (1) 111. With compounds of amidine structure (2) they react under the conditions of the Schotten-Baumann reaction to give almost quantitatively 2-hydroxy-s-triazines (3) 121. 2-Hydroxy-~-triazines with two different hydrocarbon radicals in the 4-and the 6-position can also be prepared in this way. C1 CI CC13 CI
π SIMILAR VOLUMES
Cyanornethylated and cyanoethylated secondary aliphatic amines ( I ) are converted by chlorination at 20-50 C cia isolable dichloro derivatives (2) into highly reactive non-isol-aminopropionitrile], or conjugated bicycles [e. 9. (7) from 3-pyrrolidinopropionitrile]. Still further chlorination betwe