ChemInform Abstract: Conversion of N-Alkyldiisopropylamines into N,N-Bis(5-chloro-3-oxo[1,2]dithiol-4-yl)amines.
β Scribed by Susana Barriga; Lidia S. Konstantinova; Carlos F. Marcos; Oleg A. Rakitin; Charles W. Rees; Tomas Torroba; Andrew J. P. White; David J. Williams
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Conversion of N-Alkyldiisopropylamines into N, 2]dithiol-4-yl)amines.
-Reaction of N-alkyldiisopropylamines (I) and (IV) with excess S 2 Cl 2 and excess DABCO followed by hydrolysis with formic acid provides a novel way to N-alkylated N,N-bis(1,2-dithiol-4-yl)amines (II) and (V). Side products are the known tricyclic bis(dithiolo)thiazines (VI) except for the triisopropylamine (I), where the tricyclic product is sterically forbidden. The structure of compound (Va) is studied in detail using X-ray crystallographic analysis.
π SIMILAR VOLUMES
The title compounds were prepared from 1,3,4,6tetrathiapentalene-2,5-dione (1) in one step via the in situ The X-ray single crystal structure of (Et 4 N) 2 [Zn(dmid) 2 ] (3 a) gave the tetragonal space group P4 3 2 1 2 with a = b = 13.810(2) A Γ , c = 16.480(3) A Γ , and Z = 4. (n-Bu 4 N) 2 [Zn(dmi