Heterocyclization of hydrazine with acetaldehyde and H2S |
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Authors: | Akhmetova V R Nadyrgulova G R Murzakova N N Starikova Z A Antipin M Yu Kunakova R V |
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Institution: | 1.Institute of Petrochemistry and Catalysis, Russian Academy of Sciences, 141 prosp. Oktyabrya, 450075, Ufa, Russian Federation ;2.A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation ; |
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Abstract: | Hydrazine is regioselectively condensed with a mixture of acetaldehyde and H2S at a temperature below −10 °C to form 2,4,6,8-tetramethyl-3,7-dithia-1,5-diazabicyclo3.3.0]-octane. The reaction at 0 °C
with the reverse order of mixing of the starting reagents affords 2,4,6-trimethyl(1,3,5-dithiazinan-5-yl)amine as the major
product. |
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