Eingegangen am 21. Februar 1978 [l.n]Paracyclophanes by Vacuum Vapour Phase Pyrolysis of Disulfones By vacuum vapour phase pyrolysis of the cyclic disulfones 7-9 at 58O0C/O.01 Torr the sterically strained [l.n]paracyclophanes 1-3 were obtained in excellent yields. The lowest members of this series 1
Herstellung von Iminen durch Gasphasen-Pyrolyse: N-Methyl-äthylidenimin
✍ Scribed by J. Meier; F. Akermann; Hs. H. Günthard
- Publisher
- John Wiley and Sons
- Year
- 1968
- Tongue
- German
- Weight
- 368 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Sumnzary. N-methyl-ethylidenimine (CH,-CH=N-CH,) was obtained by pyrolysis of 2inethylaziridine (CH,-CH-CH-NH) in a gas phase flow system, using quartz as a catalyst.
Pyrolysis of aziridine (CH,-CH,-NH) gave mainly N-methyl-methylenimine (CH,=N-CH,). Under I I the conditions used in this work, pyrolysis of both compounds surprisingly showed cleavage of the CC-bond in the three-membered ring. No monomeric ethylidenimine (CH,-CH=NH) could be isolated by pyrolysis of trimeric ethylidenimine (2,4,6-trimethyl-hexahydro-l, 3,5-triazine), whereas N-vinyl-ethylidenimine (CH,-CH=N-CH=CH,) could be identified as one of the pyrolysis products. NMR. data for N-methyl-ethylidenimine and N-vinyl-ethylidenimine are given for identification purposes.
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