Study on the structures of 2-substituted iminothiazolidine derivatives
✍ Scribed by Masatoshi Sakae; Masanori Katsurada; Mayumi Watanabe; Fumio Yoneda; Sadao Nishigaki; Toshimasa Ishida
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 268 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
The reaction of 2‐bromoethylamine 1 with methylisothiocyanate 2 under mild condition gave 2‐methyl‐amino‐2‐thiazoline 3 as the major product together with two kinds of byproducts, 3‐(N‐methylthiocar‐bamoyl)‐2‐methyliminothiazolidine 4 and N,N′‐dimethyl‐N‐(2‐thiazolin‐2‐yl)thiourea 5. Thermal isomer‐ization of 5 to 4 was observed. The structures of the byproducts were confirmed by X‐ray crystallography.
📜 SIMILAR VOLUMES
The structures and stability of fullerene derivatives were obtained from the results of density functional theory calculations that were performed on 6 non-classical and 306 classical isomers of C 58 X 18 (X = H, F, Cl). The calculated results demonstrated that the most energetically stable isomers
s, 5-H). Mass spectrum, m/z: 167 (M +, 21), 132 (M + -CI, i00), 105 (46), 79 (ii), 69 (14). Compound VIII, PMR spectrum: 4.58 ppm (s, CH2CI). Mass spectrum, m/z: 201 (M +, 20), 170 (15), 166 (M + -CI i00), 105 (50), 79 (16), 69 (14). Compound VI, PMR spectrum: 2.22 ppm (s, CH3); mass spectrum, m/z: